Polypeptides having cellulase activity

ABSTRACT

The present disclosure relates to CBH II chimera fusion polypeptides, nucleic acids encoding the polypeptides, and host cells for producing the polypeptides.

CROSS REFERENCE TO RELATED APPLICATIONS

The application is a continuation application of U.S. application Ser.No. 12/755,328, filed Apr. 6, 2010 (now U.S. Pat. No. 9,249,401), whichclaims priority under 35 U.S.C. §119 to U.S. Provisional ApplicationSer. No. 61/166,993, filed, Apr. 6, 2009, and 61/177,882, filed May 13,2009, the disclosures of which are incorporated herein by reference.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH

This invention was made with Government support under Grant No. GM068664awarded by the National Institutes of Health and Grant No.DAAD19-03-0D-0004 awarded by ARO—US Army Robert Morris AcquisitionCenter. The government has certain rights in the invention.

TECHNICAL FIELD

The disclosure relates to biomolecular engineering and design, andengineered proteins and nucleic acids.

BACKGROUND

The performance of cellulase mixtures in biomass conversion processesdepends on many enzyme properties including stability, productinhibition, synergy among different cellulase components, productivebinding versus nonproductive adsorption and pH dependence, in additionto the cellulose substrate physical state and composition. Given themultivariate nature of cellulose hydrolysis, it is desirable to havediverse cellulases to choose from in order to optimize enzymeformulations for different applications and feedstocks.

SUMMARY

The disclosure provides recombinant polypeptides having cellulaseactivity and increased thermostability and activity compared to awild-type protein. The disclosure provides and demonstrates that CBHIIchimeras and the native enzymes having a Cys to Ser mutation at theC-terminal end (e.g., at about amino acid 310-315 depending upon thenative protein sequence, see, e.g., SEQ ID NO:2 and 4) hydrolyze moresolid cellulose than the native enzyme in long time hydrolysis assays.

The disclosure provides a recombinant polypeptide comprising a C→Ssubstitution in the C-terminal region in a motif comprising the sequenceGECDG (SEQ ID NO:2 from 312-316), wherein the variant comprisesincreased thermostability and cellulase activity compared to a wild-typecellobiohydrolase. For example, the disclosure provide polypeptideshaving increased thermostability and cellulase activity comprising asequence that is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:2comprising a C314S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ IDNO:4 comprising a C311S; is at least 85%, 90%, 95%, 98%, 99% identicalSEQ ID NO:12 comprising a C310S; is at least 85%, 90%, 95%, 98%, 99%identical SEQ ID NO:13 comprising a C312S; is at least 85%, 90%, 95%,98%, 99% identical SEQ ID NO:14 comprising a C314S; is at least 85%,90%, 95%, 98%, 99% identical SEQ ID NO:15 comprising a C315S; is atleast 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:16 comprising a C313S;is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:17 comprising aC311S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:19comprising a C313S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ IDNO:21 comprising a C312S; is at least 85%, 90%, 95%, 98%, 99% identicalSEQ ID NO:22 comprising a C311S; is at least 85%, 90%, 95%, 98%, 99%identical SEQ ID NO:64 comprising a C400S; is at least 85%, 90%, 95%,98%, 99% identical SEQ ID NO:65 comprising a C407S; is at least 85%,90%, 95%, 98%, 99% identical SEQ ID NO:66 comprising a C394S; is atleast 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:67 comprising a C400S;is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:68 comprising aC400S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:69comprising a C400S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ IDNO:70 comprising a C400S; is at least 85%, 90%, 95%, 98%, 99% identicalSEQ ID NO:71 comprising a C400S; is at least 85%, 90%, 95%, 98%, 99%identical SEQ ID NO:72 comprising a C400S; is at least 85%, 90%, 95%,98%, 99% identical SEQ ID NO:73 comprising a C400S; is at least 85%,90%, 95%, 98%, 99% identical SEQ ID NO:74 comprising a C400S; is atleast 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:75 comprising a C400S;is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:76 comprising aC407S; is at least 850, 900, 950, 980, 99% identical SEQ ID NO:77comprising a C394S; or is at least 850, 900, 950, 980, 99% identical SEQID NO:78 comprising a C412S, wherein the foregoing polypeptides havecellulase activity and improved thermostability compared to theircorresponding parental (wild-type) protein lacking a Cys→Ser mutation.

The disclosure also provides substantially purified polypeptides thatare either recombinantly produced, synthetic made, or otherwisenon-naturally generated wherein the polypeptide comprises a sequence asset forth below having from 1-10, 10-20 or 20-30 conservative amino acidsubstitutions except at the position identified below wherein a C→Ssubstitution is present: SEQ ID NO:2 comprising a C314S; SEQ ID NO:4comprising a C311S; SEQ ID NO:12 comprising a C310S; SEQ ID NO:13comprising a C312S; SEQ ID NO:14 comprising a C314S; SEQ ID NO:15comprising a C315S; SEQ ID NO:16 comprising a C313S; SEQ ID NO:17comprising a C311S; SEQ ID NO:19 comprising a C313S; SEQ ID NO:21comprising a C312S; SEQ ID NO:22 comprising a C311S; SEQ ID NO:64comprising a C400S; SEQ ID NO:65 comprising a C407S; SEQ ID NO:66comprising a C394S; SEQ ID NO:67 comprising a C400S; SEQ ID NO:68comprising a C400S; SEQ ID NO:69 comprising a C400S; SEQ ID NO:70comprising a C400S; SEQ ID NO:71 comprising a C400S; SEQ ID NO:72comprising a C400S; SEQ ID NO:73 comprising a C400S; SEQ ID NO:74comprising a C400S; SEQ ID NO:75 comprising a C400S; SEQ ID NO:76comprising a C407S; SEQ ID NO:77 comprising a C394S; or SEQ ID NO:78comprising a C412S.

The disclosure provides a recombinant polypeptide comprising a sequenceselected from the group consisting of: (a) a polypeptide having at least85% or greater identity to SEQ ID NO:2, having a Ser at position 314,and wherein the polypeptide has cellulase activity; (b) a polypeptidehaving at least 70% or greater identity to SEQ ID NO:4, having a Ser atposition 311, and wherein the polypeptide has cellulase activity; (c) apolypeptide having 70% or greater identity to a sequence selected fromthe group consisting of: (i) SEQ ID NO:12 and having a Ser at position310, (ii) SEQ ID NO:13 and having a Ser at position 312, (iii) SEQ IDNO:14 and having a Ser at position 314, (iv) SEQ ID NO:15 and having aSer at position 315, (v) SEQ ID NO:16 and having a Ser at position 313,(vi) SEQ ID NO:17 and having a Ser at position 311, (vii) SEQ ID NO:19and having a Ser at position 313, (viii) SEQ ID NO:21 and having a Serat position 312, and (ix) SEQ ID NO:22 and having a Ser at position 311,and wherein each of the foregoing polypeptides has cellulase activity;and (d) a chimeric polypeptide comprising at least two domains from twodifferent parental cellobiohydrolase polypeptides, wherein the domainscomprise from N- to C-terminus: (segment 1)-(segment 2)-(segment3)-(segment 4)-(segment 5)-(segment 6)-(segment 7)-(segment 8); wherein:segment 1 comprises a sequence that is at least 50-100% identity toamino acid residue from about 1 to about x₁ of SEQ ID NO:2 (“1”), SEQ IDNO:4 (“2”) or SEQ ID NO:6 (“3”); segment 2 comprises a sequence that isat least 50-100% identity to amino acid residue x₁ to about x₂ of SEQ IDNO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”); segment 3 comprisesa sequence that is at least 50-100% identity to amino acid residue x₂ toabout x₃ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”);segment 4 comprises a sequence that is at least 50-100% identity toamino acid residue x₃ to about x₄ of SEQ ID NO:2 (“1”), SEQ ID NO:4(“2”) or SEQ ID NO:6 (“3”); segment 5 comprises a sequence that is atleast 50-100% identity to about amino acid residue x₄ to about x₅ of SEQID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”); segment 6comprises a sequence that is at least 50-100% identity to amino acidresidue x₅ to about x₆ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ IDNO:6 (“3”); segment 7 comprises a sequence that is at least 50-100%identity to amino acid residue x₆ to about x₇ of SEQ ID NO:2 (“1”) orSEQ ID NO:4 (“2”); and segment 8 comprises a sequence that is at least50-100% identity to amino acid residue x₇ to about x₈ of SEQ ID NO:2(“1”) or SEQ ID NO:4 (“2”); wherein x₁ is residue 43, 44, 45, 46, or 47of SEQ ID NO:2, or residue 42, 43, 44, 45, or 46 of SEQ ID NO:4 or SEQID NO:6; x₂ is residue 70, 71, 72, 73, or 74 of SEQ ID NO:2, or residue68, 69, 70, 71, 72, 73, or 74 of SEQ ID NO:4 or SEQ ID NO:6; x₃ isresidue 113, 114, 115, 116, 117 or 118 of SEQ ID NO:2, or residue 110,111, 112, 113, 114, 115, or 116 of SEQ ID NO:4 or SEQ ID NO:6; x₄ isresidue 153, 154, 155, 156, or 157 of SEQ ID NO:2, or residue 149, 150,151, 152, 153, 154, 155 or 156 of SEQ ID NO:4 or SEQ ID NO:6; x₅ isresidue 220, 221, 222, 223, or 224 of SEQ ID NO:2, or residue 216, 217,218, 219, 220, 221, 222 or 223 of SEQ ID NO:4 or SEQ ID NO:6; x₆ isresidue 256, 257, 258, 259, 260 or 261 of SEQ ID NO:2, or residue 253,254, 255, 256, 257, 258, 259 or 260 of SEQ ID NO:4 or SEQ ID NO:6; x₇ isresidue 312, 313, 314, 315 or 316 of SEQ ID NO:2, or residue 309, 310,311, 312, 313, 314, 315 or 318 of SEQ ID NO:4; and x₈ is an amino acidresidue corresponding to the C-terminus of the polypeptide have thesequence of SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6, wherein thechimeric polypeptide comprises a Ser at position 314 of SEQ ID NO:2 orposition 311 of SEQ ID NO:4 and wherein the chimeric polypeptide hascellulase activity and improved thermostability and/or pH stabilitycompared to a CBH II polypeptide comprising SEQ ID NO:2, 4, or 6. In oneembodiment of the recombinant polypeptide segment 1 comprises amino acidresidue from about 1 to about x₁ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”)or SEQ ID NO:6 (“3”) and having 1-10 conservative amino acidsubstitutions; segment 2 is from about amino acid residue x₁ to about x₂of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”) and havingabout 1-10 conservative amino acid substitutions; segment 3 is fromabout amino acid residue x₂ to about x₃ of SEQ ID NO:2 (“1”), SEQ IDNO:4 (“2”) or SEQ ID NO:6 (“3”) and having about 1-10 conservative aminoacid substitutions; segment 4 is from about amino acid residue x₃ toabout x₄ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”)and having about 1-10 conservative amino acid substitutions; segment 5is from about amino acid residue x₄ to about x₅ of SEQ ID NO:2 (“1”),SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”) and having about 1-10conservative amino acid substitutions; segment 6 is from about aminoacid residue x₅ to about x₆ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) orSEQ ID NO:6 (“3”) and having about 1-10 conservative amino acidsubstitutions; segment 7 is from about amino acid residue x₆ to about x₇of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”) and havingabout 1-10 conservative amino acid substitutions; and segment 8 is fromabout amino acid residue x₇ to about x₈ of SEQ ID NO:2 (“1”), SEQ IDNO:4 (“2”) or SEQ ID NO:6 (“3”) and having about 1-10 conservative aminoacid substitutions except at position 314 of SEQ ID NO:2, position 311or SEQ ID NO:4 or 313 of SEQ ID NO:6. In yet another embodiment, thechimeric polypeptide comprises a sequence that is at least 80%, 90%,95%, 98% or 99% identical to a sequence selected from the groupconsisting of SEQ ID NO:12-62 and 63.

The disclosure also provides a recombinant polypeptide consisting of asequence as set forth in SEQ ID NO:12-62 or 63.

The disclosure also provides a polynucleotide encoding any of thepolypeptides as described above, vectors containing the polynucleotideand host cells containing the polynucleotide or vector.

The disclosure also provides an enzymatic preparation comprising apolypeptide of the disclosure in substantially purified form or as partof a cell lysate.

The disclosure also provides a method of treating a biomass comprisingcellulose, the method comprising contacting the biomass with apolypeptide or enzymatic preparation of the disclosure.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1A-B SDS-PAGE gel of candidate CBH II parent gene yeast expressionculture supernatants. (A) Gel Lanes (Left-to-Right): 1—H. jecorina,2—Empty vector, 3—H. insolens, 4—C. thermophilum, 5—H. jecorina(duplicate), 6—P. chrysosporium, 7—T. emersonii, 8—Empty vector(duplicate), 9—H. jecorina (triplicate). Numbers at bottom of gelrepresent concentration of reducing sugar (ug/mL) present in reactionafter 2-hr, 50° C. PASC hydrolysis assay. Subsequent SDS-PAGE comparisonwith BSA standard allowed estimation of H. insolens expression level of5-10 mg/L. (B) Shows SDS-PAGE gel analysis of S. cerevisiae CBH IIexpression culture supernatants. CBH II bands appear just below 60 kDamolecular weight standard. Lanes, left-to-right, 1—wild type H. jeco,2—H. jeco B7P3, 3—H. jeco C311S, 4—wild type C. ther, 5—wild type H.inso, 6—H. inso B7P3, 7—H. inso C314S. Numbers denote μg glucoseequivalent/mL reaction volume per mL SDCAA expression culturesupernatant equivalent produced during 100-minute incubation with PASC(1 mg/mL) at 50° C. in 50 mM sodium acetate, pH 4.8. Values for lanes1-4 have been divided by 2 to correct for twice the volume ofconcentrated culture supernatant being loaded where omitting thiscorrection would make the specific activity values for the H. insolensenzymes appear artificially low.

FIG. 2A-C shows illustrations of CBH II chimera library blockboundaries. (A) H. insolens CBH II catalytic domain ribbon diagram withblocks distinguished by color. CBH II enzyme is complexed withcellobio-derived isofagomine glycosidase inhibitor. (B) Linearrepresentation of H. insolens catalytic domain showing secondarystructure elements, disulfide bonds and block divisions denoted by blackarrows. (C) Sidechain contact map denoting contacts (side chain heavyatoms within 4.5 Å) that can be broken upon recombination. The majorityof broken contacts occur between consecutive blocks.

FIG. 3 shows a number of broken contacts (E) and number of mutationsfrom closest parent (m) for 23 secreted/active and 15 not secreted/notactive sample set chimeras.

FIG. 4 shows specific activity, normalized to pH 5.0, as a function ofpH for parent CBH II enzymes and three thermostable chimeras. Datapresented are averages for two replicates, where error bars for HJPlusand H. jeco denote values for two independent trials. 16-hr reaction,300 ug enzyme/g PASC, 50° C., 12.5 mM sodium citrate/12.5 mM sodiumphosphate buffer at pH as shown.

FIG. 5 shows long-time cellulose hydrolysis assay results (ug glucosereducing sugar equivalent/ug CBH II enzyme) for parents and thermostablechimeras across a range of temperatures. Error bars indicate standarderrors for three replicates of HJPlus and H. insolens CBH II enzymes.40-hr reaction, 100 ug enzyme/g PASC, 50 mM sodium acetate, pH 4.8.

FIG. 6 shows normalized residual activities for validation set chimerasafter a 12-h incubation at 63° C. Residual activities for CBH II enzymesin concentrated culture supernatants determined in 2-hr assay with PASCas substrate, 50° C., 25 mM sodium acetate buffer, pH 4.8.

FIG. 7 Map for parent and chimera CBH II enzyme expression vectorYep352/PGK91-1-ss. Vector pictured contains wild type H. jecorina cel6a(CBH II enzyme) gene. For both chimeric and parent CBH II enzymes, theCBD/linker amino acid sequence following the ss Lys-Arg Kex₂ site is:

(SEQ ID NO: 8) ASCSSVWGQCGGQNWSGPTCCASGSTCVYSNDYYSQCLPGAASSSSSTRAASTTSRVSPTTSRSSSATPPPGSTTTRVPPVGSGTATYS.

FIG. 8 shows Observed and predicted T₅₀ values for CBH II parents and 51CBH II chimeras. Line denotes linear regression model equation(parameters in Table 7). Parent CBH II T₅₀ values are denoted assquares.

FIG. 9A-C shows CBH II specific activities toward Avicel as a functionof temperature. (a) CBH II parent and chimera specific activities. (b)CBH II parent, C311S mutant and B7P3 single block substitution chimeraspecific activities. Reactions were run for 16 hours in 50 mM sodiumacetate, pH 4.8 with an Avicel concentration of 15 mg/mL. (c) CBH IIparent, single point mutant and single block substitution chimeraactivities (μg/glucose/mL reaction) toward avicel as a function oftemperature. Reactions were run for 150 minutes in 50 mM sodium acetate,pH 4.8 with an avicel concentration of 15 mg/mL. CBH II yeast culturesupernatants were dosed to achieve roughly equivalent reducing sugarproduct concentrations at 55° C. Data presented are averages of twoindependent replicates with error bars indicating the duplicate activityvalues for each temperature point.

FIG. 10 shows ClustalW multiple sequence alignment for block 7 fromparent 1, H. insolens and parent 3, C. thermophilum. Arrows denoteresidues changed in reversion mutants.

FIG. 11 shows T₅₀ values for 21111331 chimera point mutants. Valuesshown as average of two independent duplicates, error bars indicateduplicate T₅₀ values for each point mutant. Inactivation was carried outfor 10 minutes at the temperature being tested in 50 mM sodium acetatebuffer, pH 4.8. Residual activity was determined by incubation with 1g/L phosphoric acid swollen cellulose (PASC) in above buffer for 100minutes at 50° C.

FIG. 12 shows T₅₀ values for H. insolens and H. jecorina parent CBH IIs,Ser single point mutants and B7P3 block substitution chimeras. Valuesshown as average of three independent replicates, error bars indicateone standard deviation for each CBH II. Inactivation was carried out for10 minutes at the temperature being tested in 50 mM sodium acetatebuffer, pH 4.8. Residual activity was determined by incubation with 1g/L phosphoric acid swollen cellulose (PASC) in above buffer for 100minutes at 50° C.

FIG. 13 shows T₅₀ values for CBH II chimeras 31311112, 13231111 and thewild type CBH II catalytic domain from P. chrysosporium (fused to the H.jecorina CBM) and heterologously secreted from S. cerevisiae. Valuesshown as two independent replicates with error bars indicating valuesfor each trial. Inactivation was carried out for 10 minutes at thetemperature tested, in 50 mM sodium acetate buffer, pH 4.8. Residualactivity was determined by incubation with 1 g/L phosphoric acid swollencellulose (PASC) in above buffer for 100 minutes at 50° C.

FIG. 14A-D shows CBH II recombination block interfaces. (a) Inter-blocksites where novel non-parental residue pairs are possible (connectedspheres) are usually surface-exposed, potentially allowing solvent toscreen the interactions. (b) An example interface (B5-B6) illustratesconservation of the backbone (cartoons for aligned H. jecorina and H.insolens), variable residues on the surface, and the comparatively rarepossibility of a novel buried hydrophobic pair at residues 173 and 253(arrow). (c) Blocks 1-4 from H. jecorina (black cartoon) match cognateH. insolens blocks (color-coded cartoon) without large deviations,though movement associated with substrate binding is observed (arrow) inpart of B3 (yellow). (d) Cognate blocks 5-8 are also similar, though theindel at the B6,B7 junction (arrow) will require conformational change.

FIG. 15 shows a structural analysis of C314S mutation and itsstabilizing effect. (a) Hydrogen positions for high-resolution H.insolens structure (1ocn) were added with REDUCE.1 (b) The reconfiguredgeometry of the analogous serine structure was modeled in PyMOL(http:(//)www.pymol.org). Sidechain optimization in the SHARPEN2modeling platform (with an all-atom Rosetta energy function) alsosuggested that both the Cys314 and Ser314 would donate hydrogen bonds tothe carbonyl of Pro339, and accept hydrogen bonds from the amide ofGly316. The superior hydrogen bonding capacity of serine may play a rolein the greater stability of the serine containing variants. Anotherpossible explanation is geometric complementarity. Specifically, the Cysposition from 1ocn shows evidence of conformational strain in that thesidechain is noticeably bent (i.e. the improper dihedral angle fromN—C—Cα—Cβ is 6° from the standard position), increasing the distancefrom the Pro carbonyl. Numbers in figure not preceded by letters denotehydrogen bond distances (Å).

DETAILED DESCRIPTION

As used herein and in the appended claims, the singular forms “a,”“and,” and “the” include plural referents unless the context clearlydictates otherwise. Thus, for example, reference to “a domain” includesa plurality of such domains and reference to “the protein” includesreference to one or more proteins, and so forth.

Also, the use of “or” means “and/or” unless stated otherwise. Similarly,“comprise,” “comprises,” “comprising” “include,” “includes,” and“including” are interchangeable and not intended to be limiting.

It is to be further understood that where descriptions of variousembodiments use the term “comprising,” those skilled in the art wouldunderstand that in some specific instances, an embodiment can bealternatively described using language “consisting essentially of” or“consisting of.”

Although methods and materials similar or equivalent to those describedherein can be used in the practice of the disclosed methods andcompositions, the exemplary methods, devices and materials are describedherein.

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood to one of ordinary skill inthe art to which this disclosure belongs. Thus, as used throughout theinstant application, the following terms shall have the followingmeanings.

Recent studies have documented the superior performance of cellulasesfrom thermophilic fungi relative to their mesophilic counterparts inlaboratory scale biomass conversion processes, where enhanced stabilityleads to retention of activity over longer periods of time at bothmoderate and elevated temperatures. Fungal cellulases are attractivebecause they are highly active and can be expressed in fungal hosts suchas Hypocrea jecorina (anamorph Trichoderma reesei) at levels up to 40g/L in the supernatant. Unfortunately, the set of documentedthermostable fungal cellulases is small. In the case of the processivecellobiohydrolase class II (CBH II) enzymes, fewer than 10 naturalthermostable gene sequences are annotated in the CAZy database.

As described more fully herein, using recursive chimeric polypeptidegeneration and analysis particular stabilizing domains and ultimatelyspecific amino acid were identified the imparted thermostability andimproved activity.

As will be described in more detail below, the invention is based, atleast in part, on the generation and expression of novel enzymes thatcatalyze the hydrolysis of cellulose. In one embodiment, novelpolypeptides that have been engineered to hydrolyze cellose at increasedtemperatures are provided. Such polypeptides include cellobiohydrolasevariants that have been altered to include amino acid substitutions atspecified residues. While these variants will be described in moredetail below, it is understood that polypeptides of the disclosure maycontain one or more modified amino acids. The presence of modified aminoacids may be advantageous in, for example, (a) increasing apolypeptide's half-life, (b) thermostability, and (c) increasedsubstrate turnover. Amino acid(s) are modified, for example,co-translationally or post-translationally during recombinant production(e.g., N-linked glycosylation at N—X—S/T motifs during expression inmammalian cells) or modified by synthetic means. Accordingly, a“mutant”, “variant” or “modified” protein, enzyme, polynucleotide, gene,or cell, means a protein, enzyme, polynucleotide, gene, or cell, thathas been altered or derived, or is in some way different or changed,from a parent protein, enzyme, polynucleotide, gene, or cell. A mutantor modified protein or enzyme is usually, although not necessarily,expressed from a mutant polynucleotide or gene.

A “mutation” means any process or mechanism resulting in a mutantprotein, enzyme, polynucleotide, gene, or cell. This includes anymutation in which a protein, enzyme, polynucleotide, or gene sequence isaltered, and any detectable change in a cell arising from such amutation. Typically, a mutation occurs in a polynucleotide or genesequence, by point mutations, deletions, or insertions of single ormultiple nucleotide residues. A mutation includes polynucleotidealterations arising within a protein-encoding region of a gene as wellas alterations in regions outside of a protein-encoding sequence, suchas, but not limited to, regulatory or promoter sequences. A mutation ina gene can be “silent”, i.e., not reflected in an amino acid alterationupon expression, leading to a “sequence-conservative” variant of thegene. This generally arises when one amino acid corresponds to more thanone codon.

Non-limiting examples of a modified amino acid include a glycosylatedamino acid, a sulfated amino acid, a prenlyated (e.g., farnesylated,geranylgeranylated) amino acid, an acetylated amino acid, an acylatedamino acid, a pegylated amino acid, a biotinylated amino acid, acarboxylated amino acid, a phosphorylated amino acid, and the like.References adequate to guide one of skill in the modification of aminoacids are replete throughout the literature. Example protocols are foundin Walker (1998) Protein Protocols on CD-ROM (Humana Press, Towata,N.J.).

Recombinant methods for producing and isolating modifiedcellobiohydrolase polypeptides of the disclosure are described herein.In addition to recombinant production, the polypeptides may be producedby direct peptide synthesis using solid-phase techniques (e.g., Stewartet al. (1969) Solid-Phase Peptide Synthesis (WH Freeman Co, SanFrancisco); and Merrifield (1963) J. Am. Chem. Soc. 85: 2149-2154).Peptide synthesis may be performed using manual techniques or byautomation. Automated synthesis may be achieved, for example, usingApplied Biosystems 431A Peptide Synthesizer (Perkin Elmer, Foster City,Calif.) in accordance with the instructions provided by themanufacturer.

“Cellobiohydrolase II” or “CBH II enzyme” means an enzyme in thecellulase family 6 proteins, which are widely distributed in bacteriaand fungi. The enzymes are involved in hydrolysis of cellulose.

By “cellulase activity” means an enzyme that is capable of hydrolyzingcellulose. Cellulase refers to a class of enzymes produced by fungi,bacteria, and protozoans that catalyze the hydrolysis of cellulose.However, there are also cellulases produced by other types of organismssuch as plants and animals. The EC number for this group of enzymes isEC 3.2.1.4. There are five general types of cellulases based on the typeof reaction catalyzed: endo-cellulase; exo-cellulase, within thiscategory there are two main types of exo-cellulases (orcellobiohydrolases, abbreviate CBH)—one type working processively fromthe reducing end, and one type working processively from thenon-reducing end of cellulose; cellobiase or beta-glucosidasehydrolyses; oxidative cellulases; and cellulose phosphorylases thatdepolymerize cellulose using phosphates instead of water. Most fungalcellulases have two-domains: a catalytic domain and a cellulose bindingdomain, that are connected by a flexible linker. In specific embodimentsof the disclosure the cellulase activity is a CBH activity. Thesequences described herein include, in some instances, both thecellulose binding domain and the catalytic domain or just the catalyticdomain. In such instances where only the catalytic domain sequence isprovided it will be recognized that a cellulose binding domain (CBD)such as that provided in SEQ ID NO:8, may be functional linked (eitheras part of the coding sequence or fused later) to the catalytic domaineither directly or through a linker.

A “protein” or “polypeptide”, which terms are used interchangeablyherein, comprises one or more chains of chemical building blocks calledamino acids that are linked together by chemical bonds called peptidebonds. An “enzyme” means any substance, preferably composed wholly orlargely of protein, that catalyzes or promotes, more or lessspecifically, one or more chemical or biochemical reactions. A “native”or “wild-type” protein, enzyme, polynucleotide, gene, or cell, means aprotein, enzyme, polynucleotide, gene, or cell that occurs in nature.

An “amino acid sequence” is a polymer of amino acids (a protein,polypeptide, etc.) or a character string representing an amino acidpolymer, depending on context. The terms “protein,” “polypeptide,” and“peptide” are used interchangeably herein. “Amino acid” is a moleculehaving the structure wherein a central carbon atom is linked to ahydrogen atom, a carboxylic acid group (the carbon atom of which isreferred to herein as a “carboxyl carbon atom”), an amino group (thenitrogen atom of which is referred to herein as an “amino nitrogenatom”), and a side chain group, R. When incorporated into a peptide,polypeptide, or protein, an amino acid loses one or more atoms of itsamino acid carboxylic groups in the dehydration reaction that links oneamino acid to another. As a result, when incorporated into a protein, anamino acid is referred to as an “amino acid residue.”

A particular amino acid sequence of a given protein (i.e., thepolypeptide's “primary structure,” when written from the amino-terminusto carboxy-terminus) is determined by the nucleotide sequence of thecoding portion of a mRNA, which is in turn specified by geneticinformation, typically genomic DNA (including organelle DNA, e.g.,mitochondrial or chloroplast DNA). Thus, determining the sequence of agene assists in predicting the primary sequence of a correspondingpolypeptide and more particular the role or activity of the polypeptideor proteins encoded by that gene or polynucleotide sequence.

“Conservative amino acid substitution” or, simply, “conservativevariations” of a particular sequence refers to the replacement of oneamino acid, or series of amino acids, with essentially identical aminoacid sequences. One of skill will recognize that individualsubstitutions, deletions or additions which alter, add or delete asingle amino acid or a percentage of amino acids in an encoded sequenceresult in “conservative variations” where the alterations result in thedeletion of an amino acid, addition of an amino acid, or substitution ofan amino acid with a chemically similar amino acid.

Conservative substitution tables providing functionally similar aminoacids are well known in the art. For example, one conservativesubstitution group includes Alanine (A), Serine (S), and Threonine (T).Another conservative substitution group includes Aspartic acid (D) andGlutamic acid (E). Another conservative substitution group includesAsparagine (N) and Glutamine (Q). Yet another conservative substitutiongroup includes Arginine (R) and Lysine (K). Another conservativesubstitution group includes Isoleucine, (I) Leucine (L), Methionine (M),and Valine (V). Another conservative substitution group includesPhenylalanine (F), Tyrosine (Y), and Tryptophan (W).

Thus, “conservative amino acid substitutions” of a listed polypeptidesequence (e.g., SEQ ID NOs: 2, 4, 6, and 12-78) include substitutions ofa percentage, typically less than 10%, of the amino acids of thepolypeptide sequence, with a conservatively selected amino acid of thesame conservative substitution group. Accordingly, a conservativelysubstituted variation of a polypeptide of the disclosure can contain100, 75, 50, 25, or 10 substitutions with a conservatively substitutedvariation of the same conservative substitution group.

It is understood that the addition of sequences which do not alter theencoded activity of a nucleic acid molecule, such as the addition of anon-functional or non-coding sequence, is a conservative variation ofthe basic nucleic acid. The “activity” of an enzyme is a measure of itsability to catalyze a reaction, i.e., to “function”, and may beexpressed as the rate at which the product of the reaction is produced.For example, enzyme activity can be represented as the amount of productproduced per unit of time or per unit of enzyme (e.g., concentration orweight), or in terms of affinity or dissociation constants. As usedinterchangeably herein a “cellobiohydrolase activity or cellulaseactivity”, “biological activity of cellobiohydrolase or cellulase” or“functional activity of cellobiohydrolase or cellulase”, refers to anactivity exerted by a protein, polypeptide having cellulase activity andin specific embodiments cellobiohydrolase activity on a cellulosesubstrate, as determined in vivo, or in vitro, according to standardtechniques.

One of skill in the art will appreciate that many conservativevariations of the nucleic acid constructs which are disclosed yield afunctionally identical construct. For example, as discussed above, owingto the degeneracy of the genetic code, “silent substitutions” (i.e.,substitutions in a nucleic acid sequence which do not result in analteration in an encoded polypeptide) are an implied feature of everynucleic acid sequence which encodes an amino acid. Similarly,“conservative amino acid substitutions,” in one or a few amino acids inan amino acid sequence are substituted with different amino acids withhighly similar properties, are also readily identified as being highlysimilar to a disclosed construct. Such conservative variations of eachdisclosed sequence are a feature of the polypeptides provided herein.

“Conservative variants” are proteins or enzymes in which a given aminoacid residue has been changed without altering overall conformation andfunction of the protein or enzyme, including, but not limited to,replacement of an amino acid with one having similar properties,including polar or non-polar character, size, shape and charge. Aminoacids other than those indicated as conserved may differ in a protein orenzyme so that the percent protein or amino acid sequence similaritybetween any two proteins of similar function may vary and can be, forexample, at least 30%, at least 50%, at least 70%, at least 80%, or atleast 90%, as determined according to an alignment scheme. As referredto herein, “sequence similarity” means the extent to which nucleotide orprotein sequences are related. The extent of similarity between twosequences can be based on percent sequence identity and/or conservation.“Sequence identity” herein means the extent to which two nucleotide oramino acid sequences are invariant. “Sequence alignment” means theprocess of lining up two or more sequences to achieve maximal levels ofidentity (and, in the case of amino acid sequences, conservation) forthe purpose of assessing the degree of similarity. Numerous methods foraligning sequences and assessing similarity/identity are known in theart such as, for example, the Cluster Method, wherein similarity isbased on the MEGALIGN algorithm, as well as BLASTN, BLASTP, and FASTA(Lipman and Pearson, 1985; Pearson and Lipman, 1988). When using all ofthese programs, the preferred settings are those that results in thehighest sequence similarity.

Non-conservative modifications of a particular polypeptide are thosewhich substitute any amino acid not characterized as a conservativesubstitution. For example, any substitution which crosses the bounds ofthe six groups set forth above. These include substitutions of basic oracidic amino acids for neutral amino acids, (e.g., Asp, Glu, Asn, or Glnfor Val, Ile, Leu or Met), aromatic amino acid for basic or acidic aminoacids (e.g., Phe, Tyr or Trp for Asp, Asn, Glu or Gln) or any othersubstitution not replacing an amino acid with a like amino acid. Basicside chains include lysine (K), arginine (R), histidine (H); acidic sidechains include aspartic acid (D), glutamic acid (E); uncharged polarside chains include glycine (G), asparagine (N), glutamine (Q), serine(S), threonine (T), tyrosine (Y), cysteine (C); nonpolar side chainsinclude alanine (A), valine (V), leucine (L), isoleucine (I), proline(P), phenylalanine (F), methionine (M), tryptophan (W); beta-branchedside chains include threonine (T), valine (V), isoleucine (I); aromaticside chains include tyrosine (Y), phenylalanine (F), tryptophan (W),histidine (H).

A “parent” protein, enzyme, polynucleotide, gene, or cell, is anyprotein, enzyme, polynucleotide, gene, or cell, from which any otherprotein, enzyme, polynucleotide, gene, or cell, is derived or made,using any methods, tools or techniques, and whether or not the parent isitself native or mutant. A parent polynucleotide or gene encodes for aparent protein or enzyme.

In addition to providing variants of CBH II polypeptides, chimericpolypeptides that comprise: 1) a variant domain isolated from a firstparental strand and modified to include an amino acid substitution; and2) a domain isolated from a second parental strand either unmodified ormodified to include a new activity or an activity that a complements thedomain, are provided. Methods for engineering a chimeric polypeptide ofthe disclosure are disclosed herein.

The disclosure provides cellulase and cellobiohydrolase (CBH) IIvariants, mutants and chimeras having increased thermostability comparedto a wild-type or parental protein, wherein the wild-type proteinconsisting of SEQ ID NO:2, 4 or 6. The variant comprises a Serine in theC-terminal region in a motif comprising the sequence GEXDG, wherein X isC, A or G (SEQ ID NO:107), wherein X is substituted with Serine, thevariant comprising cellulase activity and wherein the polypeptide hasincreased thermostability compared to a wild-type cellulase lacking aserine in the sequence GEXDG (SEQ ID NO:107). In one embodiment, thevariants comprise at least a mutation of a Cys-Ser in the motif GECDG(see, e.g., SEQ ID NO:2 from amino acid 312-316) found in most cellulaseand cellobiohydrolase II proteins (as described more fully below) andmay comprise additional mutations that improve thermostability oractivity. The identity between cellulases can be quite low. The serinesubstitution as described above is applicable to any cellulase havingthe motif of SEQ ID NO:107 (e.g., wherein the polypeptide has at least60% or greater identity to SEQ ID NO:2 or 4).

For example, the disclosure provide polypeptides having increasedthermostability and cellulase activity comprising a sequence that is atleast 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:2 comprising a C314S;is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:4 comprising aC311S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:12comprising a C310S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ IDNO:13 comprising a C312S; is at least 85%, 90%, 95%, 98%, 99% identicalSEQ ID NO:14 comprising a C314S; is at least 85%, 90%, 95%, 98%, 99%identical SEQ ID NO:15 comprising a C315S; is at least 85%, 90%, 95%,98%, 99% identical SEQ ID NO:16 comprising a C313S; is at least 85%,90%, 95%, 98%, 99% identical SEQ ID NO:17 comprising a C311S; is atleast 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:19 comprising a C313S;is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:21 comprising aC312S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:22comprising a C311S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ IDNO:64 comprising a C400S; is at least 85%, 90%, 95%, 98%, 99% identicalSEQ ID NO:65 comprising a C407S; is at least 85%, 90%, 95%, 98%, 99%identical SEQ ID NO:66 comprising a C394S; is at least 85%, 90%, 95%,98%, 99% identical SEQ ID NO:67 comprising a C400S; is at least 85%,90%, 95%, 98%, 99% identical SEQ ID NO:68 comprising a C400S; is atleast 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:69 comprising a C400S;is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:70 comprising aC400S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ ID NO:71comprising a C400S; is at least 85%, 90%, 95%, 98%, 99% identical SEQ IDNO:72 comprising a C400S; is at least 85%, 90%, 95%, 98%, 99% identicalSEQ ID NO:73 comprising a C400S; is at least 85%, 90%, 95%, 98%, 99%identical SEQ ID NO:74 comprising a C400S; is at least 85%, 90%, 95%,98%, 99% identical SEQ ID NO:75 comprising a C400S; is at least 85%,90%, 950, 980, 99% identical SEQ ID NO:76 comprising a C407S; is atleast 850, 900, 950, 980, 99% identical SEQ ID NO:77 comprising a C394S;or is at least 850, 900, 950, 980, 99% identical SEQ ID NO:78 comprisinga C412S, wherein the foregoing polypeptides have cellulase activity andimproved thermostability compared to their corresponding parental(wild-type) protein lacking a Cys→Ser mutation.

In yet another embodiment, the disclosure provides polypeptide asdescribed above, however, they further comprise at least one additionmutation that can be determined by alignment to SEQ ID NO:64, whereinSEQ ID NO:64 comprises a Pro at position 413, or a Ser or Thr atposition 231, or a Ser or Thr at position 305, or a Gln or Asn atposition 410, or a Glu at position 82, or any combination of theforegoing. Similar substitutions can be identified by sequence alignmentof the amino acid sequence of SEQ ID NO:64 with those of SEQ ID NOs:2,4, 6, 12-63, and 65-78.

The disclosure also provides substantially purified polypeptides thatare either recombinantly produced, synthetic made, or otherwisenon-naturally generated wherein the polypeptide comprise a sequence asset forth below having from 1-10, 10-20 or 20-30 conservative amino acidsubstitutions except at the position identified below wherein a C→Ssubstitution is present:

SEQ ID NO:2 comprising a C314S;SEQ ID NO:4 comprising a C311S;SEQ ID NO:12 comprising a C310S;SEQ ID NO:13 comprising a C312S;SEQ ID NO:14 comprising a C314S;SEQ ID NO:15 comprising a C315S;SEQ ID NO:16 comprising a C313S;SEQ ID NO:17 comprising a C311S;SEQ ID NO:19 comprising a C313S;SEQ ID NO:21 comprising a C312S;SEQ ID NO:22 comprising a C311S;SEQ ID NO:64 comprising a C400S;SEQ ID NO:65 comprising a C407S;SEQ ID NO:66 comprising a C394S;SEQ ID NO:67 comprising a C400S;SEQ ID NO:68 comprising a C400S;SEQ ID NO:69 comprising a C400S;SEQ ID NO:70 comprising a C400S;SEQ ID NO:71 comprising a C400S;SEQ ID NO:72 comprising a C400S;SEQ ID NO:73 comprising a C400S;SEQ ID NO:74 comprising a C400S;SEQ ID NO:75 comprising a C400S;SEQ ID NO:76 comprising a C407S;SEQ ID NO:77 comprising a C394S; orSEQ ID NO:78 comprising a C412S.

“Isolated polypeptide” refers to a polypeptide which is separated fromother contaminants that naturally accompany it, e.g., protein, lipids,and polynucleotides. The term embraces polypeptides which have beenremoved or purified from their naturally-occurring environment orexpression system (e.g., host cell or in vitro synthesis).

“Substantially pure polypeptide” refers to a composition in which thepolypeptide species is the predominant species present (i.e., on a molaror weight basis it is more abundant than any other individualmacromolecular species in the composition), and is generally asubstantially purified composition when the object species comprises atleast about 50 percent of the macromolecular species present by mole or% weight. Generally, a substantially pure polypeptide composition willcomprise about 60% or more, about 70% or more, about 80% or more, about90% or more, about 95% or more, and about 98% or more of allmacromolecular species by mole or % weight present in the composition.In some embodiments, the object species is purified to essentialhomogeneity (i.e., contaminant species cannot be detected in thecomposition by conventional detection methods) wherein the compositionconsists essentially of a single macromolecular species. Solventspecies, small molecules (<500 Daltons), and elemental ion species arenot considered macromolecular species.

“Reference sequence” refers to a defined sequence used as a basis for asequence comparison. A reference sequence may be a subset of a largersequence, for example, a segment of a full-length gene or polypeptidesequence. Generally, a reference sequence can be at least 20 nucleotideor amino acid residues in length, at least 25 nucleotide or residues inlength, at least 50 nucleotides or residues in length, or the fulllength of the nucleic acid or polypeptide. Since two polynucleotides orpolypeptides may each (1) comprise a sequence (i.e., a portion of thecomplete sequence) that is similar between the two sequences, and (2)may further comprise a sequence that is divergent between the twosequences, sequence comparisons between two (or more) polynucleotides orpolypeptides are typically performed by comparing sequences of the twopolynucleotides or polypeptides over a “comparison window” to identifyand compare local regions of sequence similarity.

“Sequence identity” means that two amino acid sequences aresubstantially identical (i.e., on an amino acid-by-amino acid basis)over a window of comparison. The term “sequence similarity” refers tosimilar amino acids that share the same biophysical characteristics. Theterm “percentage of sequence identity” or “percentage of sequencesimilarity” is calculated by comparing two optimally aligned sequencesover the window of comparison, determining the number of positions atwhich the identical residues (or similar residues) occur in bothpolypeptide sequences to yield the number of matched positions, dividingthe number of matched positions by the total number of positions in thewindow of comparison (i.e., the window size), and multiplying the resultby 100 to yield the percentage of sequence identity (or percentage ofsequence similarity). With regard to polynucleotide sequences, the termssequence identity and sequence similarity have comparable meaning asdescribed for protein sequences, with the term “percentage of sequenceidentity” indicating that two polynucleotide sequences are identical (ona nucleotide-by-nucleotide basis) over a window of comparison. As such,a percentage of polynucleotide sequence identity (or percentage ofpolynucleotide sequence similarity, e.g., for silent substitutions orother substitutions, based upon the analysis algorithm) also can becalculated. Maximum correspondence can be determined by using one of thesequence algorithms described herein (or other algorithms available tothose of ordinary skill in the art) or by visual inspection.

As applied to polypeptides, the term substantial identity or substantialsimilarity means that two peptide sequences, when optimally aligned,such as by the programs BLAST, GAP or BESTFIT using default gap weightsor by visual inspection, share sequence identity or sequence similarity.Similarly, as applied in the context of two nucleic acids, the termsubstantial identity or substantial similarity means that the twonucleic acid sequences, when optimally aligned, such as by the programsBLAST, GAP or BESTFIT using default gap weights (described elsewhereherein) or by visual inspection, share sequence identity or sequencesimilarity.

One example of an algorithm that is suitable for determining percentsequence identity or sequence similarity is the FASTA algorithm, whichis described in Pearson, W. R. & Lipman, D. J., (1988) Proc. Natl. Acad.Sci. USA 85:2444. See also, W. R. Pearson, (1996) Methods Enzymology266:227-258. Preferred parameters used in a FASTA alignment of DNAsequences to calculate percent identity or percent similarity areoptimized, BL50 Matrix 15: −5, k-tuple=2; joining penalty=40,optimization=28; gap penalty −12, gap length penalty=−2; and width=16.

Another example of a useful algorithm is PILEUP. PILEUP creates amultiple sequence alignment from a group of related sequences usingprogressive, pairwise alignments to show relationship and percentsequence identity or percent sequence similarity. It also plots a treeor dendogram showing the clustering relationships used to create thealignment. PILEUP uses a simplification of the progressive alignmentmethod of Feng & Doolittle, (1987) J. Mol. Evol. 35:351-360. The methodused is similar to the method described by Higgins & Sharp, CABIOS5:151-153, 1989. The program can align up to 300 sequences, each of amaximum length of 5,000 nucleotides or amino acids. The multiplealignment procedure begins with the pairwise alignment of the two mostsimilar sequences, producing a cluster of two aligned sequences. Thiscluster is then aligned to the next most related sequence or cluster ofaligned sequences. Two clusters of sequences are aligned by a simpleextension of the pairwise alignment of two individual sequences. Thefinal alignment is achieved by a series of progressive, pairwisealignments. The program is run by designating specific sequences andtheir amino acid or nucleotide coordinates for regions of sequencecomparison and by designating the program parameters. Using PILEUP, areference sequence is compared to other test sequences to determine thepercent sequence identity (or percent sequence similarity) relationshipusing the following parameters: default gap weight (3.00), default gaplength weight (0.10), and weighted end gaps. PILEUP can be obtained fromthe GCG sequence analysis software package, e.g., version 7.0 (Devereauxet al., (1984) Nuc. Acids Res. 12:387-395).

Another example of an algorithm that is suitable for multiple DNA andamino acid sequence alignments is the CLUSTALW program (Thompson, J. D.et al., (1994) Nuc. Acids Res. 22:4673-4680). CLUSTALW performs multiplepairwise comparisons between groups of sequences and assembles them intoa multiple alignment based on sequence identity. Gap open and Gapextension penalties were 10 and 0.05 respectively. For amino acidalignments, the BLOSUM algorithm can be used as a protein weight matrix(Henikoff and Henikoff, (1992) Proc. Natl. Acad. Sci. USA89:10915-10919).

As mentioned above, cellobiohydrolase and cellulase family members canbe identified by sequence alignment and a substitution in the motifGECDG (see, e.g., SEQ ID NO:2 from amino acid 312-316) made. Themodified polypeptide may then be assayed for activity as described belowat various temperatures and conditions to identify those modificationsthat introduce a favorable activity. Exemplary sequences can be found inthe following GenBank accession numbers, the sequences of which areincorporated herein by reference.

P07987 Q6E5B1 GUX2_TRIRE Q6E5B1_9AGAR Q9NEY8 B7X9Z0 Q9HEY8_TRIREB7X9Z0_COPCI Q7LSP2 A8NEJ3 Q7LSP2_TRIKO A8NEJ3_COPC7 Q6UJX9 Q96V98Q6UJX9_TRIVI Q96V98_ORPSP A3QVU7 Q7Z7X6 A3QVU7_TRIVI Q727X6_PIREQ 1HCL5Q870B2 Q1HCL5_TRIKO Q870B2_9FUNG Q66PN1 Q874E1 Q66PN1_9HYPO Q874E1_ORPSPB5TWC7 A9FHT2 B5TWC7_9HYPO A9FHT2_SORC5 Q9C1S9 BOFEV9 GUX6_HUMINBOFEV9_9FUNG Q2GMP2 Q6EY63 Q2GMP2_CHAGB Q6EY63_9FUNG A7E6G7 Q6EH22A7E6G7_SCLS1 Q6EH22_NEOFR Q0UPA5 B6EA50 Q0UPA5_PHANO B6EA50_NEOPA A6S7A6B0FEV4 A6S7A6_BOTFB B0FEV4_NEOPA P49075 6EIY8 GUX3_AGABI Q6EIY8_NEOFRQ02321 Q9UW10 Q02321_PHACH Q9UW10_9FUNG Q9C1R4 Q12646 Q9C1R4_LENEDQ12646_NEOPA Q96VU2 Q6A4K7 Q96VU2_LENED Q6A4K7_9FUNG B2ABX7 Q9UW11B2ABX7_PODAN Q9UW11_9FUNG A4RPH6 Q9P8Q8 A4RPH6_MAGGR Q9P8Q8_9FUNG B0FEV8B0FEV8_9FUNG

In yet other embodiments, the family of variant cellulase polypeptidehaving improved thermostability include those set forth in the followingtable having a C→S, G→S or A→S substitution. In addition, polypeptideshaving 85%, 90%, 95%, 98%, or 99% sequence identity to any of thefollowing sequences having the identified substitutions in the followingtable, having cellulase activity and thermostability are alsoencompassed by the disclosure.

Alignment of amino acid frame bracketing H. jecorina CBH II Cys311 forprotein sequences having highest identity to H. jecorina CBH II.Residues at 311 equivalent position denoted by bold, underline areshown. Sequences for recombinant H. insolens and P. chrys CBH IIsstudied in this work are denoted as H inso and P. chrys. Fifty-four ofthe 250 most identical sequences were excluded due to redundancy (i.e.point mutants for structural studies or >95% identical isoforms). Theaccession number for the cellulase is identified and the correspondingsequence is incorporated herein by reference as if copied directly fromthe accession number. The sequences associated with the accessionnumbers are referred to as SEQ ID NO:79-106. A replacement of thebold-underlined residue (e.g., C, A or G) with S. The number inparenthesis following the sequence identified the SEQ ID NO:)

H.jeco ----T---G---D----S---L--LDSFVWVKPGGE C DG--T----S-------------(4)XP_001903170 ----T---G---L----D---I--EDAFVWIKPGGE CDG--T----S-------------(79) XP_001226029----T---G---H----D---L--LDAFVWIKPGGE C DG--T----S-------------(80)XP_360146 ----T---G---S----E---L--ADAFVWIKPGGE CDG--V----S-------------(81) H.inso ----T---G---H----Q---Y--VDAFVWVKPGGEC DG--T----S-------------(2) XP_001598803----T---G---D----A---L--EDAFVWVKPGGE A DG--T----S-------------(82)XP_001796781 ----T---D---D----P---L--LDAYVWVKPGGE GDG--T----S-------------(83) AAA50608----T---G---S----S---L--IDAIVWVKPGGE C DG--T----S-------------(84)AAK28357 ----T---G---S----S---L--IDSIVWVKPGGE CDG--T----S-------------(85) BAH59082----T---G---S----P---L--IDSIVWVKPGGE C DG--T----S-------------(86)AAT64008 ----T---G---S----S---L--IDAIVWIKPGGE CDG--T----T-------------(87) P.crys ----T---G---S----Q---F--IDSIVWVKPGGEC DG--T----S-------------(12) BAH59083----T---P---S----S---L--IDSIVWVKPGGE A DG--T----S-------------(88)XP_001833045 ----T---P---S----S---A--IDAIVWIKPGGE ADG--T----S-------------(89) XP_002391276----T---G---S----S---L--IDSIVWVKPGGE------------------------(90)AAD51055 ----P---D---S----SKP-L--LDAYMWIKTPGE ADG--S----S-------------(91) ABY52798----S---G---Y----P---L--LDAFMWLKTPGE A DG--S----A-------------(92)AAF34679 ----P---D---ASMP-L---L--LDAYMWLKTPGE ADG--S----A-------------(93) ABY52797----P---S---K----P---L--LDAYMWIKTPGE A DG--S----S-------------(94)AAR08200 ----PNP-G---M----P---L--LDAYMWLKTPGE ADG--S----S-------------(95) AAB92678----P---N---P----GSMPL--LDAYMWIKTPGE A DG--S----S-------------(96)ABY52799 ----S---P---DPEKFP---L--LDAYFWLKPPGE ADG--S----D-------------(97) AA060491----T---G---D----A---N--IDAYLWVKPPGE A DG---------------------(98)AA009068 ----V---K---M----P---L--LDAYMWLKTPGE ADG--S----D-------------(99) ZP_04371095----T---G---D----A---A--VDAFLWIKPPGE A DG--C----A-------------(100)ZP_03818362 ----T---G---D----S---Q--IDAFLWVKIVGE ADG---------------------(101) ZP_03817628----T---G---D----P---Q--IDAFLWVKIPGE A DG---------------------(102)ZP_04331392 ----T---G---N----P---L--IDAFIWTKLPGE ADG---------------------(103) 2BOE-X ----T---G---D----P---M--IDAFLWIKLPGEA DG---------------------(104) ZP_04608509----T---G---D----S---A--IAAYLWVKLPGE A DG---------------------(105)P26414 ----T---G---D----P---A--IDAFLWIKPPGE ADG---------------------(106)

For the purposes of the disclosure, a polypeptide of the disclosureexhibits improved thermostability with respect to a corresponding parentpolypeptide if it has a T₅₀ which is at least about 4° C., or at leastabout 9° C. higher than that of the parent cellulase, or for example acellobiohydrolase having a T₅₀ from about 4° C. to about 30° C. higher,or any amount therebetween, or a T₅₀ from about 9° C. to about 30° C.higher, or any amount therebetween, when compared to that of the parentcellobiohydrolase. The T₅₀ is the temperature at which the modified orthe natural enzyme retains 50% of its residual activity after apre-incubation for 15 minutes and is determined by the assay detailed inExamples below or as known in the art.

The modified cellobiohydrolases or cellulases of the disclosure may haveT₅₀ which is about 4° C. to about 30° C. higher than that of acorresponding parent cellobiohydrolase (e.g., SEQ ID NO:2, 4 or 6), orany range therebetween, about 5° C. to about 20° C. higher, or any rangetherebetween, about 8° C. to about 15° C. higher, or any rangetherebetween, or from about 9° C. to about 15° C. higher, or any rangetherebetween. For example, the modified cellulase may have a T₅₀ that isat least about 4, 5, 6, 7, 8, 9, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28,or 30° C. higher than that of the corresponding parentcellobiohydrolase.

The variants identified herein can also be used to generate chimericcellobiohydrolases. For example, SCHEMA has been used previously tocreate families of hundreds of active β-lactamase and cytochrome P450enzyme chimeras. SCHEMA uses protein structure data to define boundariesof contiguous amino acid “blocks” which minimize <E>, the libraryaverage number of amino acid sidechain contacts that are broken when theblocks are swapped among different parents. It has been shown that theprobability that a β-lactamase chimera was folded and active wasinversely related to the value of E for that sequence. The RASPP(Recombination as Shortest Path Problem) algorithm was used to identifythe block boundaries that minimized <E> relative to the library averagenumber of mutations, <m>. More than 20% of the ˜500 unique chimerascharacterized from a β-lactamase collection comprised of 8 blocks from 3parents (3⁸=6,561 possible sequences) were catalytically active. Asimilar approach produced a 3-parent, 8-block cytochrome P450 chimerafamily containing more than 2,300 novel, catalytically active enzymes.Chimeras from these two collections were characterized by high numbersof mutations, 66 and 72 amino acids on average from the closest parent,respectively. SCHEMA/RASPP thus enabled design of chimera familieshaving significant sequence diversity and an appreciable fraction offunctional members.

It has also been shown that the thermostabilities of SCHEMA chimeras canbe predicted based on sequence-stability data from a small sample of thesequences. Linear regression modeling of thermal inactivation data for184 cytochrome P450 chimeras showed that SCHEMA blocks made additivecontributions to thermostability. More than 300 chimeras were predictedto be thermostable by this model, and all 44 that were tested were morestable than the most stable parent. It was estimated that as few as 35thermostability measurements could be used to predict the mostthermostable chimeras. Furthermore, the thermostable P450 chimerasdisplayed unique activity and specificity profiles, demonstrating thatchimeragenesis can lead to additional useful enzyme properties. HereSCHEMA recombination of CBH II enzymes can generate chimeric cellulasesthat are active on phosphoric acid swollen cellulose (PASC) at hightemperatures, over extended periods of time, and broad ranges of pH.

Using the methods described herein a number of chimeric polypeptideshaving cellobiohydrolases activity were generated having improvedcharacteristics compared to the wild-type parental CBH II proteins.

A diverse family of novel CBH II enzymes was constructed by swappingblocks of sequence from three fungal CBH II enzymes. Twenty-three of 48chimeric sequences sampled from this set were secreted in active form byS. cerevisiae, and five have half-lives at 63° C. that were greater thanthe most stable parent. Given that this 48-member sample set representsless than 1% of the total possible 6,561 sequences, we predict that thisone collection of chimeras already contains hundreds of active,thermostable CBH II enzymes, a number that dwarfs the approximatelytwenty fungal CBH II enzymes in the CAZy database.

The approach of using the sample set sequence-stability data to identifyblocks that contribute positively to chimera thermostability wasvalidated by finding that all 10 catalytically active chimeras in thesecond CBH II validation set were more thermostable than the most stableparent, a naturally-thermostable CBH II from the thermophilic fungus, H.insolens. This disclosure has thus far generated a total of 33 new CBHII enzymes that are expressed in catalytically active form in S.cerevisiae, 15 of which are more thermostable than the most stableparent from which they were constructed. These 15 thermostable enzymesare diverse in sequence, differing from each other and their closestnatural homologs at as many as 94 and 58 amino acid positions,respectively.

Analysis of the thermostabilities of CBH II chimeras in the combinedsample and validation sets indicates that the four thermostabilizingblocks identified, B1P1, B6P3, B7P3 and B8P2, make cumulativecontributions to thermal stability when present in the same chimera.Four of the five sample set chimeras that are more thermostable than theH. insolens CBH II contain either two or three of these stabilizingblocks (Table 1). The ten active members of the validation set, all ofwhich are more stable than the H. insolens enzyme, contain at least twostabilizing blocks, with five of the six most thermostable chimeras inthis group containing either three or four stabilizing blocks.

The disclosure demonstrates that stabilizing blocks can be recombined tocreate novel highly stable, active cellulases. The stability regressionmodel predicts that the CBH II SCHEMA library contains 2,026 chimerasthat are more stable than the most stable parent enzyme. These chimerasare diverse and distinct from the native cellulases: they differ fromthe parents by between 8 and 72 mutations (an average of 50) and fromeach other by an average of 63 mutations. A total of 33 genes from thisset were synthesized and expressed in S. cerevisiae: every one of thesechimeric CBH IIs was found to be more stable than the most stable parentcellulase, from the thermophilic fungus H. insolens, as measured eitherby its half-life of inactivation at 63° C. or T₅₀. Reducing the sequencecomplexity by making chimeras of only eight blocks allowed thegeneration of a sequence-stability model and identification of a singlehighly stabilizing sequence block. By testing only ten amino acidsubstitutions in this block a single, highly stabilizing substitutionwas identified. The very large stabilizing effect of the C313S (withreference to SEQ ID NO:6; C314S, SEQ ID NO:2 and C311S, SEQ ID NO:4)substitution observed across the chimeras and in the native P.chrysosporium, H. insolens and H. jecorina CBH II enzymes suggests thatmutation of any residue at this position to Ser may stabilize any family6 cellulase into which it is introduced.

Minimizing the number of broken contacts upon recombination (FIG. 2C)allows the blocks to be approximated as decoupled units that makeindependent contributions to the stability of the entire protein, thusleading to cumulative or even additive contributions to chimerathermostability. For this CBH II enzyme recombination, SCHEMA waseffective in minimizing such broken contacts: whereas there are 303total interblock contacts defined in the H. insolens parent CBH IIcrystal structure, the CBH II SCHEMA library design results in only 33potential broken contacts. Given that the CBH II enzyme parents do notfeature obvious structural subdomains, and only four of the eight blocks(1, 5, 7 and 8) resemble compact structural units, or modules, the lownumber of broken contacts demonstrates that the SCHEMA/RASPP algorithmis effective for cases in which the number of blocks appears greaterthan the number of structural subdivisions. As previously observed forβ-lactamase and cytochrome P450 chimeras, low E values were predictiveof chimera folding and activity. Although not used here, thisrelationship should be valuable for designing chimera sample sets thatcontain a high fraction of active members.

The disclosure also used chimera to determine if the pH stability couldbe improved in CBH II enzymes. Whereas the specific activity of H.jecorina CBH II declines sharply as pH increases above the optimum valueof 5, HJPlus, created by substituting stabilizing blocks onto the mostindustrially relevant H. jecorina CBH II enzyme, retains significantlymore activity at these higher pHs (FIG. 4). The thermostable 11113132and 13311332 chimeras, and also the H. insolens and C. thermophilum CBHII cellulase parents, have even broader pH/activity profiles thanHJPlus. The narrow pH/activity profile of H. jecorina CBH II has beenattributed to the deprotonation of several carboxyl-carboxylate pairs,which destabilizes the protein above pH ˜6. The substitution of parent 3in block 7 in HJPlus changes aspartate 277 to histidine, eliminating thecarboxyl-carboxylate pair between D277 and D316 (of block 8). ReplacingD277 with the positively charged histidine may prevent destabilizingcharge repulsion at nonacidic pH, allowing HJPlus to retain activity athigher pH than H. jecorina CBH II. The even broader pH/activity profilesof the remaining two thermostable chimeras and the H. insolens and C.thermophilum parent CBH II enzymes may be due to the absence of acidicresidues at positions corresponding to the E57-E119 carboxyl-carboxylatepair of HJPlus and H. jecorina CBH II.

HJPlus exhibits both relatively high specific activity and highthermostability. FIG. 5 shows that these properties lead to goodperformance in long-time hydrolysis experiments: HJPlus hydrolyzedcellulose at temperatures 7-15° C. higher than the parent CBH II enzymesand also had a significantly increased long-time activity relative toall the parents at their temperature optima, bettering H. jecorina CBHII by a factor of 1.7. Given that the specific activity of the HJPluschimera is less than that of the H. jecorina CBH II parent, thisincreased long-time activity can be attributed to the ability of thethermostable HJPlus to retain activity at optimal hydrolysistemperatures over longer reaction timer.

The other two thermostable chimeras shared HJPlus's broad temperaturerange. This observation supports a positive correlation between t_(1/2)at elevated temperature and maximum operating temperature, and suggeststhat many of the thermostable chimeras among the 6,561 CBH II chimerasequences will also be capable of degrading cellulose at elevatedtemperatures. While this ability to hydrolyze the amorphous PASCsubstrate at elevated temperatures bodes well for the potential utilityof thermostable fungal CBH II chimeras, studies with more challengingcrystalline substrates and substrates containing lignin will provide amore complete assessment of this novel CBH II enzyme family's relevanceto biomass degradation applications.

The majority of biomass conversion processes use mixtures of fungalcellulases (primarily CBH II, cellobiohydrolase class I (CBH I),endoglucanases and β-glucosidase) to achieve high levels of cellulosehydrolysis. Generating a diverse group of thermostable CBH II enzymechimeras is the first step in building an inventory of stable, highlyactive cellulases from which enzyme mixtures can be formulated andoptimized for specific applications and feedstocks.

“Peptide segment” refers to a portion or fragment of a largerpolypeptide or protein. A peptide segment need not on its own havefunctional activity, although in some instances, a peptide segment maycorrespond to a domain of a polypeptide wherein the domain has its ownbiological activity. A stability-associated peptide segment is a peptidesegment found in a polypeptide that promotes stability, function, orfolding compared to a related polypeptide lacking the peptide segment. Adestabilizing-associated peptide segment is a peptide segment that isidentified as causing a loss of stability, function or folding whenpresent in a polypeptide.

“Fused,” “operably linked,” and “operably associated” are usedinterchangeably herein to broadly refer to a chemical or physicalcoupling of two otherwise distinct domains or peptide segments, whereineach domain or peptide segment when operably linked can provide afunctional polypeptide having a desired activity. Domains or peptidesegments can be connected through peptide linkers such that they arefunctional or can be fused through other intermediates or chemicalbonds. For example, two domains can be part of the same coding sequence,wherein the polynucleotides are in frame such that the polynucleotidewhen transcribed encodes a single mRNA that when translated comprisesboth domains as a single polypeptide. Alternatively, both domains can beseparately expressed as individual polypeptides and fused to one anotherusing chemical methods. Typically, the coding domains will be linked“in-frame” either directly of separated by a peptide linker and encodedby a single polynucleotide. Various coding sequences for peptide linkersand peptide are known in the art.

“Polynucleotide” or “nucleic acid sequence” refers to a polymeric formof nucleotides. In some instances a polynucleotide refers to a sequencethat is not immediately contiguous with either of the coding sequenceswith which it is immediately contiguous (one on the 5′ end and one onthe 3′ end) in the naturally occurring genome of the organism from whichit is derived. The term therefore includes, for example, a recombinantDNA which is incorporated into a vector; into an autonomouslyreplicating plasmid or virus; or into the genomic DNA of a prokaryote oreukaryote, or which exists as a separate molecule (e.g., a cDNA)independent of other sequences. The nucleotides of the disclosure can beribonucleotides, deoxyribonucleotides, or modified forms of eithernucleotide. A polynucleotides as used herein refers to, among others,single- and double-stranded DNA, DNA that is a mixture of single- anddouble-stranded regions, single- and double-stranded RNA, and RNA thatis mixture of single- and double-stranded regions, hybrid moleculescomprising DNA and RNA that may be single-stranded or, more typically,double-stranded or a mixture of single- and double-stranded regions. Theterm polynucleotide encompasses genomic DNA or RNA (depending upon theorganism, i.e., RNA genome of viruses), as well as mRNA encoded by thegenomic DNA, and cDNA.

“Nucleic acid segment,” “oligonucleotide segment” or “polynucleotidesegment” refers to a portion of a larger polynucleotide molecule. Thepolynucleotide segment need not correspond to an encoded functionaldomain of a protein; however, in some instances the segment will encodea functional domain of a protein. A polynucleotide segment can be about6 nucleotides or more in length (e.g., 6-20, 20-50, 50-100, 100-200,200-300, 300-400 or more nucleotides in length). A stability-associatedpeptide segment can be encoded by a stability-associated polynucleotidesegment, wherein the peptide segment promotes stability, function, orfolding compared to a polypeptide lacking the peptide segment.

“Chimera” refers to a combination of at least two segments of at leasttwo different parent proteins. As appreciated by one of skill in theart, the segments need not actually come from each of the parents, as itis the particular sequence that is relevant, and not the physicalnucleic acids themselves. For example, a chimeric fungal class IIcellobiohydrolases (CBH II cellulases) will have at least two segmentsfrom two different parent CBH II polypeptides. The two segments areconnected so as to result in a new polypeptide having cellulaseactivity. In other words, a protein will not be a chimera if it has theidentical sequence of either one of the full length parents. A chimericpolypeptide can comprise more than two segments from two differentparent proteins. For example, there may be 2, 3, 4, 5-10, 10-20, or moreparents for each final chimera or library of chimeras. The segment ofeach parent polypeptide can be very short or very long, the segments canrange in length of contiguous amino acids from 1 to 90%, 95%, 98%, or99% of the entire length of the protein. In one embodiment, the minimumlength is 10 amino acids. In one embodiment, a single crossover point isdefined for two parents. The crossover location defines where oneparent's amino acid segment will stop and where the next parent's aminoacid segment will start. Thus, a simple chimera would only have onecrossover location where the segment before that crossover locationwould belong to one parent and the segment after that crossover locationwould belong to the second parent. In one embodiment, the chimera hasmore than one crossover location. For example, 2, 3, 4, 5, 6, 7, 8, 9,10, 11-30, or more crossover locations. How these crossover locationsare named and defined are both discussed below. In an embodiment wherethere are two crossover locations and two parents, there will be a firstcontiguous segment from a first parent, followed by a second contiguoussegment from a second parent, followed by a third contiguous segmentfrom the first parent. Contiguous is meant to denote that there isnothing of significance interrupting the segments. These contiguoussegments are connected to form a contiguous amino acid sequence. Forexample, a CBH II chimera from Humicola insolens (hereinafter “1”) andH. jecorina (hereinafter “2”), with two crossovers at 100 and 150, couldhave the first 100 amino acids from 1, followed by the next 50 from 2,followed by the remainder of the amino acids from 1, all connected inone contiguous amino acid chain. Alternatively, the CBH II chimera couldhave the first 100 amino acids from 2, the next 50 from 1 and theremainder followed by 2. As appreciated by one of skill in the art,variants of chimeras exist as well as the exact sequences. Thus, not100% of each segment need be present in the final chimera if it is avariant chimera. The amount that may be altered, either throughadditional residues or removal or alteration of residues will be definedas the term variant is defined. Of course, as understood by one of skillin the art, the above discussion applies not only to amino acids butalso nucleic acids which encode for the amino acids.

The disclosure describes in addition to specific variants, variants thatcan be used to generate CBH II chimeras. A directed SCHEMA recombinationlibrary was used to generate cellobiohydrolase enzymes based on aparticularly well-studied member of this diverse enzyme family, and moreparticularly cellobiohydrolase II enzymes: H. insolens is parent “1”(SEQ ID NO:2), H. jecorina is parent “2” (SEQ ID NO:4) and C.thermophilum is parent “3” (SEQ ID NO:6). SCHEMA is a computationalbased method for predicting which fragments of homologous proteins canbe recombined without affecting the structural integrity of the protein(see, e.g., Meyer et al., (2003) Protein Sci., 12:1686-1693). Thiscomputational approached identified seven recombination points in theCBH II parental proteins, thereby allowing the formation of a library ofCBH II chimera polypeptides, where each polypeptide comprise eightsegments. Chimeras with higher stability are identifiable by determiningthe additive contribution of each segment to the overall stability,either by use of linear regression of sequence-stability data, or byreliance on consensus analysis of the MSAs of folded versus unfoldedproteins. SCHEMA recombination ensures that the chimeras retainbiological function and exhibit high sequence diversity by conservingimportant functional residues while exchanging tolerant ones.

Thus, as illustrated by various embodiments herein, the disclosureprovides CBH II polypeptides comprising a chimera of parental domains ofwhich a parental strand or the resulting chimeric coding sequence may bemodified to comprise a C→S substitution as described above. In someembodiments, the polypeptide comprises a chimera having a plurality ofdomains from N- to C-terminus from different parental CBH II proteins:(segment 1)-(segment 2)-(segment 3)-(segment 4)-(segment 5)-(segment6)-(segment 7)-(segment 8);

wherein segment 1 comprises amino acid residue from about 1 to about x₁of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”): segment 2is from about amino acid residue x₁ to about x₂ of SEQ ID NO:2 (“1”),SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”); segment 3 is from about aminoacid residue x₂ to about x₃ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) orSEQ ID NO:6 (“3”); segment 4 is from about amino acid residue x₃ toabout x₄ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”);segment 5 is from about amino acid residue x₄ to about x₅ of SEQ ID NO:2(“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”); segment 6 is from aboutamino acid residue x₅ to about x₆ of SEQ ID NO:2 (“1”), SEQ ID NO:4(“2”) or SEQ ID NO:6 (“3”); segment 7 is from about amino acid residuex₆ to about x₇ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6(“3”); and segment 8 is from about amino acid residue x₇ to about x₈ ofSEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”);

wherein: x₁ is residue 43, 44, 45, 46, or 47 of SEQ ID NO:2, or residue42, 43, 44, 45, or 46 of SEQ ID NO:4 or SEQ ID NO:6; x₂ is residue 70,71, 72, 73, or 74 of SEQ ID NO:2, or residue 68, 69, 70, 71, 72, 73, or74 of SEQ ID NO:4 or SEQ ID NO:6; x₃ is residue 113, 114, 115, 116, 117or 118 of SEQ ID NO:2, or residue 110, 111, 112, 113, 114, 115, or 116of SEQ ID NO:4 or SEQ ID NO:6; x₄ is residue 153, 154, 155, 156, or 157of SEQ ID NO:2, or residue 149, 150, 151, 152, 153, 154, 155 or 156 ofSEQ ID NO:4 or SEQ ID NO:6; x₅ is residue 220, 221, 222, 223, or 224 ofSEQ ID NO:2, or residue 216, 217, 218, 219, 220, 221, 222 or 223 of SEQID NO:4 or SEQ ID NO:6; x₆ is residue 256, 257, 258, 259, 260 or 261 ofSEQ ID NO:2, or residue 253, 254, 255, 256, 257, 258, 259 or 260 of SEQID NO:4 or SEQ ID NO:6; x₇ is residue 312, 313, 314, 315 or 316 of SEQID NO:2, or residue 309, 310, 311, 312, 313, 314, 315 or 318 of SEQ IDNO:4 or SEQ ID NO:6; and x₈ is an amino acid residue corresponding tothe C-terminus of the polypeptide have the sequence of SEQ ID NO:2, SEQID NO:4 or SEQ ID NO:6.

Using the foregoing domain references a number of chimeric structurewere generated as set forth in Table 1. 1,588 CBH II chimera sequenceswith T₅₀ values predicted to be greater than the measured T₅₀ value of64.8 C for the H. insolens parent CBH II.

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3131333112231133 11332333 13112231 31132331 21113232 22112332 13223133 3133333213211333 11121233 13132232 13222333 21123333 13131231 13322133 3133333122131131 22331331 13111331 33323132 33321132 22121132 11311132 1132113233223332 21113332 13131332 33323131 33321131 22121131 11311131 1132113123111332 21113331 13131331 23122332 11111332 23121332 11222332 1132313233223331 21133332 21212132 23122331 11111331 23121331 11222331 1132313133322332 22211132 21212131 11113332 11131332 11111132 11331132 1132133223111331 21133331 21232132 11113331 11131331 11111131 11331131 1132133133322331 22211131 21232131 11133332 13321232 11131132 21121332 1122113223131332 22231132 12313332 12211132 13321231 11131131 21121331 1122113123131331 22231131 12313331 11133331 22223332 22323332 13123132 2132113233222132 23211332 12333332 12211131 22223331 22323331 13123131 2132113133222131 23211331 12333331 21221232 22322332 22223132 21223332 1332113212223232 23231332 33121132 21221231 22322331 22223131 21223331 1332113112223231 23231331 33121131 12231132 31121132 22322132 21322332 1112113212322232 21112132 12213132 12231131 31121131 22322131 21322331 1112113112322231 21112131 12213131 13211332 22222132 23223332 12121132 1132333232221332 21132132 12312132 13211331 22222131 23223331 12121131 1132333132221331 23323232 12312131 13231332 23311132 23322332 13121332 1122313222313332 21132131 21223232 13231331 23311131 23322331 13121331 1122313122313331 23323231 21223231 11112132 23222332 11313332 21222132 1132213222333332 11323133 21322232 11112131 23222331 11313331 21222131 1132213122333331 22321232 12233132 11132132 23331132 11333332 12323332 1122133231122332 31311132 21322231 32321132 11213332 11333331 12323331 1122133131122331 22321231 12233131 13323232 23331131 23222132 12223132 2132313213321133 31311131 12332132 11132131 11213331 23222131 12223131 2132313113222232 31222332 12332131 32321131 11312332 11213132 12322132 2132133213222231 31222331 13213332 13323231 11312331 11213131 12322131 2132133122213132 31331132 13213331 33321332 11233332 11312132 13223332 2122113222213131 31331131 13312332 33321331 11233331 11312131 13223331 2122113122312132 12113132 13312331 31123132 11332332 11233132 13322332 1332313222312131 12113131 13233332 31123131 11332331 11233131 13322331 1332313122233132 21123232 13233331 33221132 11121232 11332132 13222132 1232113222233131 21123231 13332332 33221131 11121231 11332131 13222131 1232113122332132 12133132 13332331 23313132 31323332 22221332 12221332 1332133222332131 12133131 13121232 12321232 11212132 22221331 12221331 1332133123213332 13113332 13121231 23313131 31323331 31323132 23121132 1112313223213331 13113331 32323132 12321231 11212131 31323131 23121131 1112313123312332 13133332 32323131 23333132 11232132 21122332 11122332 1322113223312331 13133331 22122332 23333131 11232131 21122331 11122331 1322113123233332 23221232 22122331 11123232 31223132 11211332 22323132 1112133223233331 23221231 33323332 11123231 21111132 11211331 22323131 1112133123332332 11311232 13212132 31121332 31223131 11231332 23323332 2332113223332331 11321333 33323331 31121331 31322132 11231331 23323331 2332113123121232 11311231 13212131 13221232 21111131 11323232 23223132 1122333223121231 11331232 13232132 13221231 31322131 11323231 23223131 1122333123212132 11331231 13232131 22311132 21131132 31321332 23322132 1132233223212131 13112132 12211332 22311131 21131131 31321331 23322131 1132233123232132 13112131 12211331 22222332 11223232 12123332 11313132 1122213223232131 13132132 12231332 22222331 11223231 12123331 11313131 1122213122211332 13132131 12231331 22331132 11322232 31221132 11333132 2112113222211331 12111332 33223132 22331131 11322231 31221131 11333131 2112113111121133 12111331 23111132 23311332 31221332 21313132 22321332 2132333222231332 11221133 33223131 23311331 31221331 21313131 22321331 2132333122231331 12131332 33322132 23331332 21313332 21333132 21123332 2122313222323232 12131331 23111131 23331331 21313331 21333131 21123331 2122313131313132 33123132 33322131 21113132 21333332 12122132 22221132 2132213222323231 33123131 12323232 21113131 21333331 12122131 22221131 2132213131313131 21212332 12323231 21133132 12122332 13122332 23221332 1312113221112332 21212331 23131132 21133131 12122331 13122331 23221331 1312113121112331 21232332 23131131 23211132 21213132 11221232 11311332 2122133231333132 21232331 11112332 23211131 21213131 11221231 11311331 2122133131333131 32121132 11112331 23231132 21312132 21311332 21122132 1232313221132332 13123232 11132332 23231131 21312131 21311331 21122131 1232313121132331 32121131 32321332 11212332 21233132 21331332 11331332 1332333223223232 13123231 11132331 11212331 21233131 21331331 11331331 1332333123223231 33121332 32321331 11232332 21332132 21211132 11211132 1322313223322232 33121331 31123332 11232331 21332131 21211131 11211131 1322313123322231 12213332 31123331 31223332 13111132 21231132 11231132 1332213211313232 12213331 32221132 21111332 13111131 21231131 11231131 1332213111323333 12312332 13223232 31223331 13131132 13313132 31321132 1232133211313231 12312331 32221131 31322332 13131131 13313131 31321131 1232133111333232 12233332 13223231 21111331 21211332 13333132 12123132 1112333211333231 12233331 13322232 31322331 21211331 13333131 12123131 1112333131311332 12332332 13322231 21131332 21231332 22123132 13123332 1222113231311331 12332331 22313132 21131331 21231331 22123131 13123331 1222113131331332 23113132 22313131 31222132 12313132 23123332 11321232 1322133231331331 12121232 22333132 31222131 12313131 23123331 11321231 1322133112113332 23113131 33221332 23321232 21323232 12311132 13122132 1112213212113331 12121231 22333131 23321231 21323231 12311131 13122131 1112213111223133 23133132 33221331 13113132 12333132 12222332 12121332 2332313211322133 23133131 23313332 13113131 12333131 21321232 12121331 2332313112133332 32323332 23313331 13133132 13313332 12222331 21311132 2232113212133331 12212132 31122132 13133131 13313331 21321231 21311131 2232113122221232 32323331 23333332 11321133 13333332 12331132 21222332 2332133231211132 12212131 31122131 11222232 13333331 12331131 21222331 2332133122221231 21321133 23333331 11222231 22123332 13311332 21331132 2112313231211131 21222232 23213132 21213332 22123331 13311331 21331131 2112313131231132 21222231 12221232 21213331 13213132 23122132 12223332 2322113231231131 12232132 23213131 21312332 13213131 23122131 12223331 2322113112112132 12232131 23312132 21312331 13312132 13331332 12322332 1211213113212332 12221231 21233332 13312131 13331331 12322331 21122232 1321233123312131 21233331 13233132 11113132 23123132 21122231 13232332 2323313221332332 13233131 11113131 23123131 12132132 13232331 23233131 1211113213332132 11133132 12222132 12132131 32223132 23332132 21332331 1333213111133131 12222131 13112332 22111132 23332131 12111131 12311332 2212133213311132 13112331 32223131 22311332 21121232 12311331 22121331 1331113113132332 32322132 22311331 21121231 22122132 13211132 13222332 1313233122111131 11122232 12131132 22122131 13211131 13222331 32123132 3232213122331332 12131131 12331332 13231132 13331132 11211232 22131132 1112223113111332 12331331 13231131 13331131

Referring to the table above, each digit refers to a domain of achimeric CBH II polypeptide. The number denotes the parental strand thedomain was derived from. For example, a chimeric CBH II chimericpolypeptide having the sequence 12111131, indicates that the polypeptidecomprises a sequence from the N-terminus to the C-terminus of: aminoacids from about 1 to x₁ of SEQ ID NO:2 (“1”) linked to amino acids fromabout x₁ to x₂ of SEQ ID NO:4 (“2”) linked to amino acids from about x₂to about x₃ of SEQ ID NO:2 linked to amino acids from about x₃ to aboutx₄ of SEQ ID NO:2 linked to amino acids from about x₄ to about x₅ of SEQID NO:2 linked to amino acids from about x₅ to about x₆ of SEQ ID NO:2linked to amino acids from about x₆ to x₇ of SEQ ID NO:6 (“3”) linked toamino acids from about x₇ to x₈ (e.g., the C-terminus) of SEQ ID NO:2.

In some embodiments, the CBH II polypeptide has a chimeric segmentstructure selected from the group consisting of 11113132, 21333331,21311131, 22232132, 33133132, 33213332, 13333232, 12133333, 13231111,11313121, 11332333, 12213111, 23311333, 13111313, 31311112, 23231222,33123313, 22212231, 21223122, 21131311, 23233133, 31212111 and 32333113.

In some embodiments, the polypeptide has improved thermostabilitycompared to a wild-type polypeptide of SEQ ID NO:2, 4, or 6. Theactivity of the polypeptide can be measured with any one or combinationof substrates as described in the examples. As will be apparent to theskilled artisan, other compounds within the class of compoundsexemplified by those discussed in the examples can be tested and used.

In some embodiments, the polypeptide can have various changes to theamino acid sequence with respect to a reference sequence. The changescan be a substitution, deletion, or insertion of one or more aminoacids. Where the change is a substitution, the change can be aconservative, a non-conservative substitution, or a combination ofconservative and non-conservative substitutions. For example, thechimera can comprises a C→S substitution at C314 of SEQ ID NO:2 or C311of SEQ ID NO:4.

Thus, in some embodiments, the polypeptides can comprise a generalstructure from N-terminus to C-terminus: (segment 1)-(segment2)-(segment 3)-(segment 4)-(segment 5)-(segment 6)-(segment 7)-(segment8),

wherein segment 1 comprises amino acid residue from about 1 to about x₁of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”) and having1-10 conservative amino acid substitutions; segment 2 is from aboutamino acid residue x₁ to about x₂ of SEQ ID NO:2 (“1”), SEQ ID NO:4(“2”) or SEQ ID NO:6 (“3”) and having about 1-10 conservative amino acidsubstitutions; segment 3 is from about amino acid residue x₂ to about x₃of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”) and havingabout 1-10 conservative amino acid substitutions; segment 4 is fromabout amino acid residue x₃ to about x₄ of SEQ ID NO:2 (“1”), SEQ IDNO:4 (“2”) or SEQ ID NO:6 (“3”) and having about 1-10 conservative aminoacid substitutions; segment 5 is from about amino acid residue x₄ toabout x₅ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”)and having about 1-10 conservative amino acid substitutions; segment 6is from about amino acid residue x₅ to about x₆ of SEQ ID NO:2 (“1”),SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”) and having about 1-10conservative amino acid substitutions; segment 7 is from about aminoacid residue x₆ to about x₇ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) orSEQ ID NO:6 (“3”) and having about 1-10 conservative amino acidsubstitutions; and segment 8 is from about amino acid residue x₇ toabout x₈ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”)and having about 1-10 conservative amino acid substitutions;

wherein x₁ is residue 43, 44, 45, 46, or 47 of SEQ ID NO:2, or residue42, 43, 44, 45, or 46 of SEQ ID NO:4 or SEQ ID NO:6; x₂ is residue 70,71, 72, 73, or 74 of SEQ ID NO:2, or residue 68, 69, 70, 71, 72, 73, or74 of SEQ ID NO:4 or SEQ ID NO:6; x₃ is residue 113, 114, 115, 116, 117or 118 of SEQ ID NO:2, or residue 110, 111, 112, 113, 114, 115, or 116of SEQ ID NO:4 or SEQ ID NO:6; x₄ is residue 153, 154, 155, 156, or 157of SEQ ID NO:2, or residue 149, 150, 151, 152, 153, 154, 155 or 156 ofSEQ ID NO:4 or SEQ ID NO:6; x₅ is residue 220, 221, 222, 223, or 224 ofSEQ ID NO:2, or residue 216, 217, 218, 219, 220, 221, 222 or 223 of SEQID NO:4 or SEQ ID NO:6; x₆ is residue 256, 257, 258, 259, 260 or 261 ofSEQ ID NO:2, or residue 253, 254, 255, 256, 257, 258, 259 or 260 of SEQID NO:4 or SEQ ID NO:6; x₇ is residue 312, 313, 314, 315 or 316 of SEQID NO:2, or residue 309, 310, 311, 312, 313, 314, 315 or 318 of SEQ IDNO:4 or SEQ ID NO:6; and x₈ is an amino acid residue corresponding tothe C-terminus of the polypeptide have the sequence of SEQ ID NO:2, SEQID NO:4 or SEQ ID NO:6 and wherein the chimera has an algorithm as setforth in Table 1 and wherein the chimera comprises a C→S substitutioncorresponding to C314 of SEQ ID NO:2 or C311 of SEQ ID NO:4.

In some embodiments, the number of substitutions can be 2, 3, 4, 5, 6,8, 9, or 10, or more amino acid substitutions (e.g., 10-20, 21-30, 31-40and the like amino acid substitutions).

In some embodiments, the functional CBH II polypeptides can havecellulase activity along with increased thermostability, such as for adefined substrate discussed in the Examples, and also have a level ofamino acid sequence identity to a reference cellobiohydrolase, orsegments thereof. The reference enzyme or segment, can be that of awild-type (e.g., naturally occurring) or an engineered enzyme. Thus, insome embodiments, the polypeptides of the disclosure can comprise ageneral structure from N-terminus to C-terminus:

wherein segment 1 comprises a sequence that is at least 50-100% identityto amino acid residue from about 1 to about x₁ of SEQ ID NO:2 (“1”), SEQID NO:4 (“2”) or SEQ ID NO:6 (“3”); segment 2 comprises a sequence thatis at least 50-100% identity to amino acid residue x₁ to about x₂ of SEQID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”); segment 3comprises a sequence that is at least 50-100% identity to amino acidresidue x₂ to about x₃ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ IDNO:6 (“3”); segment 4 comprises a sequence that is at least 50-100%identity to amino acid residue x₃ to about x₄ of SEQ ID NO:2 (“1”), SEQID NO:4 (“2”) or SEQ ID NO:6 (“3”); segment 5 comprises a sequence thatis at least 50-100% identity to about amino acid residue x₄ to about x₅of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”); segment 6comprises a sequence that is at least 50-100% identity to amino acidresidue x₅ to about x₆ of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ IDNO:6 (“3”); segment 7 comprises a sequence that is at least 50-100%identity to amino acid residue x₆ to about x₇ of SEQ ID NO:2 (“1”), SEQID NO:4 (“2”) or SEQ ID NO:6 (“3”); and segment 8 comprises a sequencethat is at least 50-100% identity to amino acid residue x₇ to about x₈of SEQ ID NO:2 (“1”), SEQ ID NO:4 (“2”) or SEQ ID NO:6 (“3”);

wherein x₁ is residue 43, 44, 45, 46, or 47 of SEQ ID NO:2, or residue42, 43, 44, 45, or 46 of SEQ ID NO:4 or SEQ ID NO:6; x₂ is residue 70,71, 72, 73, or 74 of SEQ ID NO:2, or residue 68, 69, 70, 71, 72, 73, or74 of SEQ ID NO:4 or SEQ ID NO:6; x₃ is residue 113, 114, 115, 116, 117or 118 of SEQ ID NO:2, or residue 110, 111, 112, 113, 114, 115, or 116of SEQ ID NO:4 or SEQ ID NO:6; x₄ is residue 153, 154, 155, 156, or 157of SEQ ID NO:2, or residue 149, 150, 151, 152, 153, 154, 155 or 156 ofSEQ ID NO:4 or SEQ ID NO:6; x₅ is residue 220, 221, 222, 223, or 224 ofSEQ ID NO:2, or residue 216, 217, 218, 219, 220, 221, 222 or 223 of SEQID NO:4 or SEQ ID NO:6; x₆ is residue 256, 257, 258, 259, 260 or 261 ofSEQ ID NO:2, or residue 253, 254, 255, 256, 257, 258, 259 or 260 of SEQID NO:4 or SEQ ID NO:6; x₇ is residue 312, 313, 314, 315 or 316 of SEQID NO:2, or residue 309, 310, 311, 312, 313, 314, 315 or 318 of SEQ IDNO:4 or SEQ ID NO:6; and x₈ is an amino acid residue corresponding tothe C-terminus of the polypeptide have the sequence of SEQ ID NO:2, SEQID NO:4 or SEQ ID NO:6 and wherein the chimera has an algorithm as setforth in Table 1 and wherein the chimera comprises a C→S substitutioncorresponding to C314 of SEQ ID NO:2 or C311 of SEQ ID NO:4.

In some embodiments, each segment of the chimeric polypeptide can haveat least 60%, 70%, 80%, 90%, 95%, 96%, 97%, 98%, or 99% or more sequenceidentity as compared to the reference segment indicated for each of the(segment 1), (segment 2), (segment 3), (segment 4)-(segment 5), (segment6), (segment 7), and (segment 8) of SEQ ID NO:2, SEQ ID NO:4, or SEQ IDNO:6.

In some embodiments, the polypeptide variants can have improvedthermostability compared to the enzyme activity of the wild-typepolypeptide of SEQ ID NO:2, 4, or 6 and wherein the chimera comprises aC→S substitution corresponding to C314 of SEQ ID NO:2 or C311 of SEQ IDNO:4.

The chimeric enzymes described herein may be prepared in various forms,such as lysates, crude extracts, or isolated preparations. Thepolypeptides can be dissolved in suitable solutions; formulated aspowders, such as an acetone powder (with or without stabilizers); or beprepared as lyophilizates. In some embodiments, the polypeptide can bean isolated polypeptide.

In some embodiments, the polypeptides can be in the form of arrays. Theenzymes may be in a soluble form, for example, as solutions in the wellsof mircotitre plates, or immobilized onto a substrate. The substrate canbe a solid substrate or a porous substrate (e.g, membrane), which can becomposed of organic polymers such as polystyrene, polyethylene,polypropylene, polyfluoroethylene, polyethyleneoxy, and polyacrylamide,as well as co-polymers and grafts thereof. A solid support can also beinorganic, such as glass, silica, controlled pore glass (CPG), reversephase silica or metal, such as gold or platinum. The configuration of asubstrate can be in the form of beads, spheres, particles, granules, agel, a membrane or a surface. Surfaces can be planar, substantiallyplanar, or non-planar. Solid supports can be porous or non-porous, andcan have swelling or non-swelling characteristics. A solid support canbe configured in the form of a well, depression, or other container,vessel, feature, or location. A plurality of supports can be configuredon an array at various locations, addressable for robotic delivery ofreagents, or by detection methods and/or instruments.

The disclosure also provides polynucleotides encoding the engineered CBHII polypeptides disclosed herein. The polynucleotides may be operativelylinked to one or more heterologous regulatory or control sequences thatcontrol gene expression to create a recombinant polynucleotide capableof expressing the polypeptide. Expression constructs containing aheterologous polynucleotide encoding the CBH II chimera can beintroduced into appropriate host cells to express the polypeptide.

Given the knowledge of specific sequences of the CBH II chimera enzymes(e.g., the segment structure of the chimeric CBH II), the polynucleotidesequences will be apparent form the amino acid sequence of theengineered CBH II chimera enzymes to one of skill in the art. Theknowledge of the codons corresponding to various amino acids coupledwith the knowledge of the amino acid sequence of the polypeptides allowsthose skilled in the art to make different polynucleotides encoding thepolypeptides of the disclosure. Thus, the disclosure contemplates eachand every possible variation of the polynucleotides that could be madeby selecting combinations based on possible codon choices, and all suchvariations are to be considered specifically disclosed for any of thepolypeptides described herein.

In some embodiments, the polynucleotides encode the polypeptidesdescribed herein but have about 80% or more sequence identity, about 85%or more sequence identity, about 90% or more sequence identity, about91% or more sequence identity, about 92% or more sequence identity,about 93% or more sequence identity, about 94% or more sequenceidentity, about 95% or more sequence identity, about 96% or moresequence identity, about 97% or more sequence identity, about 98% ormore sequence identity, or about 99% or more sequence identity at thenucleotide level to a reference polynucleotide encoding the CBH IIvariant of chimera polypeptides and having a C→S substitution asdescribed above (e.g., wherein the polypeptide or chimera comprises aC→S substitution corresponding to C314 of SEQ ID NO:2 or C311 of SEQ IDNO:4).

In some embodiments, the isolated polynucleotides encoding thepolypeptides may be manipulated in a variety of ways to provide forexpression of the polypeptide. Manipulation of the isolatedpolynucleotide prior to its insertion into a vector may be desirable ornecessary depending on the expression vector. The techniques formodifying polynucleotides and nucleic acid sequences utilizingrecombinant DNA methods are well known in the art. Guidance is providedin Sambrook et al., 2001, Molecular Cloning: A Laboratory Manual, 3rdEd., Cold Spring Harbor Laboratory Press; and Current Protocols inMolecular Biology, Ausubel. F. ed., Greene Pub. Associates, 1998,updates to 2007.

In some embodiments, the polynucleotides are operatively linked tocontrol sequences for the expression of the polynucleotides and/orpolypeptides. In some embodiments, the control sequence may be anappropriate promoter sequence, which can be obtained from genes encodingextracellular or intracellular polypeptides, either homologous orheterologous to the host cell. For bacterial host cells, suitablepromoters for directing transcription of the nucleic acid constructs ofthe present disclosure, include the promoters obtained from the E. colilac operon, Bacillus subtilis xylA and xylB genes, Bacillus megatariumxylose utilization genes (e.g., Rygus et al., (1991) Appl. Microbiol.Biotechnol. 35:594-599; Meinhardt et al., (1989) Appl. Microbiol.Biotechnol. 30:343-350), prokaryotic beta-lactamase gene (Villa-Kamaroffet al., (1978) Proc. Natl Acad. Sci. USA 75: 3727-3731), as well as thetac promoter (DeBoer et al., (1983) Proc. Natl Acad. Sci. USA 80:21-25). Various suitable promoters are described in “Useful proteinsfrom recombinant bacteria” in Scientific American, 1980, 242:74-94; andin Sambrook et al., supra.

In some embodiments, the control sequence may also be a suitabletranscription terminator sequence, a sequence recognized by a host cellto terminate transcription. The terminator sequence is operably linkedto the 3′ terminus of the nucleic acid sequence encoding thepolypeptide. Any terminator which is functional in the host cell ofchoice may be used.

In some embodiments, the control sequence may also be a suitable leadersequence, a nontranslated region of an mRNA that is important fortranslation by the host cell. The leader sequence is operably linked tothe 5′ terminus of the nucleic acid sequence encoding the polypeptide.Any leader sequence that is functional in the host cell of choice may beused.

In some embodiments, the control sequence may also be a signal peptidecoding region that codes for an amino acid sequence linked to the aminoterminus of a polypeptide and directs the encoded polypeptide into thecell's secretory pathway. The 5′ end of the coding sequence of thenucleic acid sequence may inherently contain a signal peptide codingregion naturally linked in translation reading frame with the segment ofthe coding region that encodes the secreted polypeptide. Alternatively,the 5′ end of the coding sequence may contain a signal peptide codingregion that is foreign to the coding sequence. The foreign signalpeptide coding region may be required where the coding sequence does notnaturally contain a signal peptide coding region. Effective signalpeptide coding regions for bacterial host cells can be the signalpeptide coding regions obtained from the genes for Bacillus NClB 11837maltogenic amylase, Bacillus stearothermophilus alpha-amylase, Bacilluslicheniformis subtilisin, Bacillus licheniformis beta-lactamase,Bacillus stearothermophilus neutral proteases (nprT, nprS, nprM), andBacillus subtilis prsA. Further signal peptides are described by Simonenand Palva, (1993) Microbiol Rev 57: 109-137.

The disclosure is further directed to a recombinant expression vectorcomprising a polynucleotide encoding the engineered CBH II variant orchimera polypeptide, and one or more expression regulating regions suchas a promoter and a terminator, a replication origin, etc., depending onthe type of hosts into which they are to be introduced. In creating theexpression vector, the coding sequence is located in the vector so thatthe coding sequence is operably linked with the appropriate controlsequences for expression.

The recombinant expression vector may be any vector (e.g., a plasmid orvirus), which can be conveniently subjected to recombinant DNAprocedures and can bring about the expression of the polynucleotidesequence. The choice of the vector will typically depend on thecompatibility of the vector with the host cell into which the vector isto be introduced. The vectors may be linear or closed circular plasmids.

The expression vector may be an autonomously replicating vector, i.e., avector that exists as an extrachromosomal entity, the replication ofwhich is independent of chromosomal replication, e.g., a plasmid, anextrachromosomal element, a minichromosome, or an artificial chromosome.The vector may contain any means for assuring self-replication.Alternatively, the vector may be one which, when introduced into thehost cell, is integrated into the genome and replicated together withthe chromosome(s) into which it has been integrated. Furthermore, asingle vector or plasmid or two or more vectors or plasmids whichtogether contain the total DNA to be introduced into the genome of thehost cell, or a transposon, may be used.

In some embodiments, the expression vector of the disclosure containsone or more selectable markers, which permit easy selection oftransformed cells. A selectable marker is a gene the product of whichprovides for biocide or viral resistance, resistance to heavy metals,prototrophy to auxotrophs, and the like. Examples of bacterialselectable markers are the dal genes from Bacillus subtilis or Bacilluslicheniformis, or markers, which confer antibiotic resistance such asampicillin, kanamycin, chloramphenicol (Example 1) or tetracyclineresistance. Other useful markers will be apparent to the skilledartisan.

In another embodiment, the disclosure provides a host cell comprising apolynucleotide encoding the CBH II variant or chimera polypeptide, thepolynucleotide being operatively linked to one or more control sequencesfor expression of the polypeptide in the host cell. Host cells for usein expressing the polypeptides encoded by the expression vectors of thedisclosure are well known in the art and include, but are not limitedto, bacterial cells, such as E. coli and Bacillus megaterium; eukaryoticcells, such as yeast cells, CHO cells and the like, insect cells such asDrosophila S2 and Spodoptera Sf9 cells; animal cells such as CHO, COS,BHK, 293, and Bowes melanoma cells; and plant cells. Other suitable hostcells will be apparent to the skilled artisan. Appropriate culturemediums and growth conditions for the above-described host cells arewell known in the art.

The CBH II variant or chimera polypeptides of the disclosure can be madeby using methods well known in the art. Polynucleotides can besynthesized by recombinant techniques, such as that provided in Sambrooket al., 2001, Molecular Cloning: A Laboratory Manual, 3rd Ed., ColdSpring Harbor Laboratory Press; and Current Protocols in MolecularBiology, Ausubel. F. ed., Greene Pub. Associates, 1998, updates to 2007.Polynucleotides encoding the enzymes, or the primers for amplificationcan also be prepared by standard solid-phase methods, according to knownsynthetic methods, for example using phosphoramidite method described byBeaucage et al., (1981) Tet Lett 22:1859-69, or the method described byMatthes et al., (1984) EMBO J. 3:801-05, e.g., as it is typicallypracticed in automated synthetic methods. In addition, essentially anynucleic acid can be obtained from any of a variety of commercialsources, such as The Midland Certified Reagent Company, Midland, Tex.,The Great American Gene Company, Ramona, Calif., ExpressGen Inc.Chicago, Ill., Operon Technologies Inc., Alameda, Calif., and manyothers.

Engineered enzymes expressed in a host cell can be recovered from thecells and or the culture medium using any one or more of the well knowntechniques for protein purification, including, among others, lysozymetreatment, sonication, filtration, salting-out, ultra-centrifugation,chromatography, and affinity separation (e.g., substrate boundantibodies). Suitable solutions for lysing and the high efficiencyextraction of proteins from bacteria, such as E. coli, are commerciallyavailable under the trade name CelLytic BTM from Sigma-Aldrich of St.Louis Mo.

Chromatographic techniques for isolation of the polypeptides include,among others, reverse phase chromatography high performance liquidchromatography, ion exchange chromatography, gel electrophoresis, andaffinity chromatography. Conditions for purifying a particular enzymewill depend, in part, on factors such as net charge, hydrophobicity,hydrophilicity, molecular weight, molecular shape, etc., and will beapparent to those having skill in the art.

Descriptions of SCHEMA directed recombination and synthesis of chimericpolypeptides are described in the examples herein, as well as in Otey etal., (2006), PLoS Biol. 4(5):e112; Meyer et al., (2003) Protein Sci.,12:1686-1693; U.S. patent application Ser. No. 12/024,515, filed Feb. 1,2008; and U.S. patent application Ser. No. 12/027,885, filed Feb. 7,2008; such references incorporated herein by reference in theirentirety.

As discussed above, the polypeptide can be used in a variety ofapplications, such as, among others, biofuel generation, cellulosebreakdown and the like.

The following examples are meant to further explain, but not limited theforegoing disclosure or the appended claims.

Examples CBH II Expression Plasmid Construction

Parent and chimeric genes encoding CBH II enzymes were cloned into yeastexpression vector YEp352/PGK91-1-ass (FIG. 6). DNA sequences encodingparent and chimeric CBH II catalytic domains were designed with S.cerevisiae codon bias using GeneDesigner software (DNA2.0) andsynthesized by DNA2.0. The CBH II catalytic domain genes were digestedwith XhoI and KpnI, ligated into the vector between the XhoI and KpnIsites and transformed into E. coli XL-1 Blue (Stratagene). CBH II geneswere sequenced using primers: CBH2L (5′-GCTGAACGTGTCATCGGTTAC-3′ (SEQ IDNO:9) and RSQ3080 (5′-GCAACACCTGGCAATTCCTTACC-3′ (SEQ ID NO:10)).C-terminal His₆ parent and chimera CBH II constructs were made byamplifying the CBH II gene with forward primer CBH2LPCR(5′-GCTGAACGTGTCATCGTTACTTAG-3′ (SEQ ID NO:11)) and reverse primerscomplementary to the appropriate CBH II gene with His₆ overhangs andstop codons. PCR products were ligated, transformed and sequenced asabove.

CBH II Enzyme Expression in S. cerevisiae.

S. cerevisiae strain YDR483W BY4742 (Matα his3Δ1 leu2Δ0 lys2Δ0 ura3Δ0ΔKRE2, ATCC No. 4014317) was made competent using the EZ Yeast IITransformation Kit (Zymo Research), transformed with plasmid DNA andplated on synthetic dropout-uracil agar. Colonies were picked into 5 mLovernight cultures of synthetic dextrose casamino acids (SDCAA) media(20 g/L dextrose, 6.7 g/L Difco yeast nitrogen base, 5 g/L Bactocasamino acids, 5.4 g/L Na₂HPO₄, 8.56 g/L NaH₂PO₄.H₂O) supplemented with20 ug/mL tryptophan and grown overnight at 30° C., 250 rpm. 5 mLcultures were expanded into 40 mL SDCAA in 250 mL Tunair flasks (SheltonScientific) and shaken at 30° C., 250 rpm for 48 hours. Cultures werecentrifuged, and supernatants were concentrated to 500 uL, using anAmicon ultrafiltration cell fitted with 30-kDa PES membrane, for use int_(1/2) assays. Concentrated supernatants were brought to1 mMphenylmethylsulfonylfluoride and 0.02% NaN₃. His₆-tagged CBH II proteinswere purified using Ni-NTA spin columns (Qiagen) per the manufacturer'sprotocol and the proteins exchanged into 50 mM sodium acetate, pH 4.8,using Zeba-Spin desalting columns (Pierce). Purified proteinconcentration was determined using Pierce Coomassie Plus protein reagentwith BSA as standard. SDS-PAGE analysis was performed by loading either20 uL of concentrated culture supernatant or approximately 5 ug ofpurified CBH II enzyme onto a 7.5% Tris-HCl gel (Biorad) and stainingwith SimplyBlue safe stain (Invitrogen). CBH II supernatants or purifiedproteins were treated with EndoH (New England Biolabs) for 1 hr at 37°C. per the manufacturer's instructions. CBH II enzyme activity inconcentrated yeast culture supernatants was measured by adding 37.5 uLconcentrated culture supernatant to 37.5 uL PASC and incubating for 2 hrat 50° C. Reducing sugar equivalents formed were determined viaNelson-Somogyi assay as described below.

Half-Life, Specific Activity, pH-Activity and Long-Time CelluloseHydrolysis Measurements.

Phosphoric acid swollen cellulose (PASC) was prepared. To enhance CBH IIenzyme activity on the substrate, PASC was pre-incubated at aconcentration of 10 g/L with 10 mg/mL A. niger endoglucanase (Sigma) in50 mM sodium acetate, pH 4.8 for 1 hr at 37° C. Endoglucanase wasinactivated by heating to 95° C. for 15 minutes, PASC was washed twicewith 50 mM acetate buffer and resuspended at 10 g/L in deionzed water.

CBH II enzyme t_(1/2)s were measured by adding concentrated CBH IIexpression culture supernatant to 50 mM sodium acetate, pH 4.8 at aconcentration giving A₅₂₀ of 0.5 as measured in the Nelson-Somogyireducing sugar assay after incubation with treated PASC as describedbelow. 37.5 uL CBH II enzyme/buffer mixtures were inactivated in a waterbath at 63° C. After inactivation, 37.5 uL endoglucanase-treated PASCwas added and hydrolysis was carried out for 2 hr at 50° C. Reactionsupernatants were filtered through Multiscreen HTS plates (Millipore).Nelson-Somogyi assay log(A₅₂₀) values, obtained using a SpectraMaxmicroplate reader (Molecular Devices) corrected for backgroundabsorbance, were plotted versus time and CBH II enzyme half-livesobtained from linear regression using Microsoft Excel.

For specific activity measurements, purified CBH II enzyme was added toPASC to give a final reaction volume of 75 uL 25 mM sodium acetate, pH4.8, with 5 g/L PASC and CBH II enzyme concentration of 3 mg enzyme/gPASC. Incubation proceeded for 2 hr in a 50° C. water bath and thereducing sugar concentration determined. For pH/activity profilemeasurements, purified CBH II enzyme was added at a concentration of 300ug/g PASC in a 75 uL reaction volume. Reactions were buffered with 12.5mM sodium citrate/12.5 mM sodium phosphate, run for 16 hr at 50° C. andreducing sugar determined. Long-time cellulose hydrolysis measurementswere performed with 300 uL volumes of 1 g/L treated PASC in 100 mMsodium acetate, pH 4.8, 20 mM NaCl. Purified CBH II enzyme was added at100 ug/g PASC and reactions carried out in water baths for 40 hr priorto reducing sugar determination.

Five candidate parent genes encoding CBH II enzymes were synthesizedwith S. cerevisiae codon bias. All five contained identical N-terminalcoding sequences, where residues 1-89 correspond to the cellulosebinding module (CBM), flexible linker region and the five N-terminalresidues of the H. jecorina catalytic domain. Two of the candidate CBHII enzymes, from Humicola insolens and Chaetomium thermophilum, weresecreted from S. cerevisiae at much higher levels than the other three,from Hypocrea jecorina, Phanerochaete chrysosporium and Talaromycesemersonii (FIG. 1). Because bands in the SDS-PAGE gel for the threeweakly expressed candidate parents were difficult to discern, activityassays in which concentrated culture supernatants were incubated withphosphoric acid swollen cellulose (PASC) were performed to confirm thepresence of active cellulase. The values for the reducing sugar formed,presented in FIG. 1, confirmed the presence of active CBH II inconcentrated S. cerevisiae culture supernatants for all enzymes exceptT. emersonii CBH II. H. insolens and C. thermophilum sequences werechose to recombine with the most industrially relevant fungal CBH IIenzyme, from H. jecorina. The respective sequence identities of thecatalytic domains are 64% (1:2), 66% (2:3) and 82% (1:3), where H.insolens is parent 1, H. jecorina is parent 2 and C. thermophilum isparent 3. These respective catalytic domains contain 360, 358 and 359amino acid residues.

Heterologous protein expression in the filamentous fungus H. jecorina,the organism most frequently used to produce cellulases for industrialapplications, is much more arduous than in Saccharomyces cerevisiae. Theobserved secretion of H. jecorina CBH II from S. cerevisiae motivatedthe choice of this heterologous host. To minimize hyperglycosylation,which has been reported to reduce the activity of recombinantcellulases, the recombinant CBH II genes were expressed in aglycosylation-deficient dKRE2 S. cerevisiae strain. This strain isexpected to attach smaller mannose oligomers to both N-linked andO-linked glycosylation sites than wild type strains, which more closelyresembles the glycosylation of natively produced H. jecorina CBH IIenzyme. SDS-PAGE gel analysis of the CBH II proteins, both with andwithout EndoH treatment to remove high-mannose structures, showed thatEndoH treatment did not increase the electrophoretic mobility of theenzymes secreted from this strain, confirming the absence of thebranched mannose moieties that wild type S. cerevisiae strains attach toglycosylation sites in the recombinant proteins.

The high resolution structure of H. insolens (pdb entry 1ocn) was usedas a template for SCHEMA to identify contacts that could be broken uponrecombination. RASPP returned four candidate libraries, each with <E>below 15. The candidate libraries all have lower <E> than previouslyconstructed chimera libraries, suggesting that an acceptable fraction offolded, active chimeras could be obtained for a relatively high <m>.Chimera sequence diversity was maximized by selecting the blockboundaries leading to the greatest <m>=50. The blocks for this designare illustrated in FIG. 2B and detailed in Table 2.

TABLE 2ClustalW multiple sequence alignment for parent CBH II enzyme catalytic domains.Blocks 2, 4, 6 and 8 are denoted by boxes and grey shading. Blocks 1, 3, 5 and 7 are notshaded. (H, inso: SEQ ID NO: 2; H. Jeco: SEQ ID NO: 4 and C. Ther: SEQ ID NO: 6).

The H. insolens CBH II catalytic domain has an α/β barrel structure inwhich the eight helices define the barrel perimeter and seven parallelβ-sheets form the active site (FIG. 2A). Two extended loops form a roofover the active site, creating a tunnel through which the substratecellulose chains pass during hydrolysis. Five of the seven blockboundaries fall between elements of secondary structure, while block 4begins and ends in the middle of consecutive α-helices (FIGS. 2A, 2B).The majority of interblock sidechain contacts occur between blocks thatare adjacent in the primary structure (FIG. 2C).

A sample set of 48 chimera genes was designed as three sets of 16chimeras having five blocks from one parent and three blocks from eitherone or both of the remaining two parents (Table 3); the sequences wereselected to equalize the representation of each parent at each blockposition. The corresponding genes were synthesized and expressed.

TABLE 3 Sequences of sample set CBH II enzyme chimeras. Inactive Active13121211 11332333 12122221 21131311 33332321 31212111 33321331 2223213221322232 33213332 21112113 23233133 31121121 13231111 32312222 1221311123223223 31311112 31313323 11113132 32121222 13111313 12121113 2131113122133222 11313121 33222333 21223122 11131231 22212231 11112321 2323122212111212 32333113 31222212 12133333 22322312 13333232 12222213 3312331312221122 21333331 22212323 23311333 23222321 33133132 32333223 33331213

Twenty-three of the 48 sample set S. cerevisiae concentrated culturesupernatants exhibited hydrolytic activity toward PASC. These resultssuggest that thousands of the 6,561 possible CBH II chimera sequences(see e.g., Table 1) encode active enzymes. The 23 active CBH II sampleset chimeras show considerable sequence diversity, differing from theclosest parental sequence and each other by at least 23 and 36 aminoacid substitutions and as many as 54 and 123, respectively. Theiraverage mutation level <m> is 36.

As Meyer et al. found correlations between E, m and the probability thata chimera is folded and active, analysis of whether similar correlationsexisted for the sample set CBH II chimeras was analyzed. The amount ofCBH II enzyme activity in concentrated expression culture supernatants,as measured by assaying for activity on PASC, was correlated to theintensity of CBH II bands in SDS-PAGE gels (FIG. 1). As with the H.jecorina CBH II parent, activity could be detected for some CBH IIchimeras with undetectable gel bands. There were no observations of CBHII chimeras presenting gel bands but lacking activity. The probabilityof a CBH II chimera being secreted in active form was inversely relatedto both E and m (FIG. 3).

Half-lives of thermal inactivation (t_(1/2)) were measured at 63° C. forconcentrated culture supernatants of the parent and active chimeric CBHII enzymes. The H. insolens, H. jecorina and C. thermophilum CBH IIparent half-lives were 95, 2 and 25 minutes, respectively (Table 1). Theactive sample set chimeras exhibited a broad range of half-lives, fromless than 1 minute to greater than 3,000. Five of the 23 active chimerashad half-lives greater than that of the most thermostable parent, H.insolens CBH II.

In attempting to construct a predictive quantitative model for CBH IIchimera half-life, five different linear regression data modelingalgorithms were used (Table 4). Each algorithm was used to construct amodel relating the block compositions of each sample set CBH II chimeraand the parents to the log(t_(1/2)). These models producedthermostability weight values that quantified a block's contribution tolog(t_(1/2)). For all five modeling algorithms, this process wasrepeated 1,000 times, with two randomly selected sequences omitted fromeach calculation, so that each algorithm produced 1,000 weight valuesfor each of the 24 blocks. The mean and standard deviation (SD) werecalculated for each block's thermostability weight. The predictiveaccuracy of each model algorithm was assessed by measuring how well eachmodel predicted the t_(1/2)s of the two omitted sequences. Thecorrelation between measured and predicted values for the 1,000algorithm iterations is the model algorithm's cross-validation score.For all five models, the cross-validation scores (X-val) were less thanor equal to 0.57 (Table 4), indicating that linear regression modelingcould not be applied to this small, 23 chimera t_(1/2) data set forquantitative CBH II chimera half-life prediction.

TABLE 4 Cross validation values for application of 5 linear regressionalgorithms to CBH II enzyme chimera block stability scores. Algorithmabbreviations: ridge regression (RR), partial least square regression(PLSR), support vector machine regression (SVMR), linear programmingsupport vector machine regression (LPSVMR) and linear programmingboosting regression (LPBoostR). Method Ridge PLS SVMR LSVM LPBoost X-val0.56 0.55 0.50 0.42 0.43

Linear regression modeling was used to qualitatively classify blocks asstabilizing, destabilizing or neutral. Each block's impact on chimerathermostability was characterized using a scoring system that accountsfor the thermostability contribution determined by each of theregression algorithms. For each algorithm, blocks with a thermostabilityweight value more than 1 SD above neutral were scored “+1”, blockswithin 1 SD of neutral were assigned zero and blocks 1 or more SD belowneutral were scored “−1”. A “stability score” for each block wasobtained by summing the 1, 0, −1 stability scores from each of the fivemodels. Table 5 summarizes the scores for each block. Block 1/parent 1(B1P1), B6P3, B7P3 and B8P2 were identified as having the greateststabilizing effects, while B1P3, B2P1, B3P2, B6P2, B7P1, B7P2 and B8P3were found to be the most strongly destabilizing blocks.

TABLE 5 Qualitative block classification results generated by fivelinear regression algorithms¹ for sample set CBH II enzyme chimeras.Score of +1 denotes a block with thermostability weight (dimensionlessmetric for contribution of a block to chimera thermostability) greaterthan one standard deviation above neutral (stabilizing), score of 0denotes block with weight within one standard deviation of neutral and−1 denotes block with weight more than one standard deviation belowneutral (destabilizing). Block Ridge PLS SVMR LSVM LPBoost Sum B1P1 1 01 1 0 3 B1P2 0 0 0 −1 0 −1 B1P3 −1 0 −1 −1 −1 −4 B2P1 −1 0 0 −1 −1 −3B2P2 1 0 0 0 0 1 B2P3 1 0 0 0 0 1 B3P1 1 0 1 0 0 2 B3P2 −1 0 −1 −1 −1 −4B3P3 1 0 1 0 0 2 B4P1 0 0 0 0 0 0 B4P2 0 0 0 0 0 0 B4P3 0 0 0 −1 0 −1B5P1 0 0 0 0 0 0 B5P2 0 0 0 0 −1 −1 B5P3 −1 0 0 −1 0 −2 B6P1 1 0 0 −1 −1−1 B6P2 −1 0 −1 −1 −1 −4 B6P3 1 1 1 1 1 5 B7P1 −1 0 −1 −1 −1 −4 B7P2 −10 −1 −1 −1 −4 B7P3 1 0 1 1 1 4 B8P1 1 0 1 −1 0 1 B8P2 1 0 1 1 0 3 B8P3−1 0 −1 −1 −1 −4

A second set of genes encoding CBH II enzyme chimeras was synthesized inorder to validate the predicted stabilizing blocks and identifycellulases more thermostable than the most stable parent. The 24chimeras included in this validation set (Table 6) were devoid of theseven blocks predicted to be most destabilizing and enriched in the fourmost stabilizing blocks, where representation was biased toward higherstability scores. Additionally, the “HJPlus” 12222332 chimera wasconstructed by substituting the predicted most stabilizing blocks intothe H. jecorina CBH II enzyme (parent 2).

TABLE 6 Sequences of 24 validation set CBH II enzyme chimeras, nine ofwhich were expressed in active form. Inactive Active 12122132 1211113112132332 12132331 12122331 12131331 12112132 12332331 13122332 1333233113111132 13331332 13111332 13311331 13322332 13311332 22122132 2231133122322132 22311332 23111332 23321131 23321332 23321331

Concentrated supernatants of S. cerevisiae expression cultures for nineof the 24 validation set chimeras, as well as the HJPlus chimera, showedactivity toward PASC (Table 6). Of the 15 chimeras for which activitywas not detected, nine contained block B4P2. Of the 16 chimerascontaining B4P2 in the initial sample set, only one showed activitytoward PASC. Summed over both chimera sets and HJPlus, just two of 26chimeras featuring B4P2 were active, indicating that this particularblock is highly detrimental to expression of active cellulase in S.cerevisiae.

The stabilities of the 10 functional chimeric CBH II enzymes from thevalidation set were evaluated. Because the stable enzymes already hadhalf-lives of more than 50 hours, residual hydrolytic activity towardPASC after a 12-hour thermal inactivation at 63° C. was used as themetric for preliminary evaluation. This 12-hour incubation produced ameasurable decrease in the activity of the sample set's mostthermostable chimera, 11113132, and completely inactivated thethermostable H. insolens parent CBH II. All ten of the functionalvalidation set chimeras retained a greater fraction of their activitiesthan the most stable parent, H. insolens CBH II.

The activities of selected thermostable chimeras using purified enzymeswas analyzed. The parent CBH II enzymes and three thermostable chimeras,the most thermostable sample set chimera 11113132, the most thermostablevalidation set chimera 13311332 and the HJPlus chimera 12222332, wereexpressed with C-terminal His₆ purification tags and purified. Tominimize thermal inactivation of CBH II enzymes during the activitytest, we used a shorter, two-hour incubation with the PASC substrate at50° C., pH 4.8. As shown in Table 3, the parent and chimera CBH IIspecific activities were within a factor of four of the most activeparent CBH II enzyme, from H. jecorina. The specific activity of HJPluswas greater than all other CBH II enzymes tested, except for H. jecorinaCBH II.

The pH dependence of cellulase activity is also important, as a broadpH/activity profile would allow the use of a CBH II chimera under awider range of potential cellulose hydrolysis conditions. H. jecorinaCBH II has been observed to have optimal activity in the pH range 4 to6, with activity markedly reduced outside these values.¹⁶ FIG. 4 showsthat the H. insolens and C. thermophilum CBH II enzymes and all threepurified thermostable CBH II chimeras have pH/activity profiles that areconsiderably broader than that of H. jecorina CBH II. Although Liu etal. report an optimal pH of 4 for C. thermophilum CBH II, the optimal pHof the recombinant enzyme here was near 7. Native H. insolens CBH II hasa broad pH/activity profile, with maximum activity around pH 9 andapproximately 60% of this maximal activity at pH 4. A similarly broadprofile was observed for the recombinant enzyme. The HJPlus chimera hasa much broader pH/activity profile than H. jecorina CBH II, showing a pHdependence similar to the other two parent CBH II enzymes.

Achieving activity at elevated temperature and retention of activityover extended time intervals are two primary motivations for engineeringhighly stable CBH II enzymes. The performance of thermostable CBH IIchimeras in cellulose hydrolysis was tested across a range oftemperatures over a 40-hour time interval. As shown in FIG. 5, all threethermostable chimeras were active on PASC at higher temperatures thanthe parent CBH II enzymes. The chimeras retained activity at 70° C.,whereas the H. jecorina CBH II did not hydrolyze PASC above 57° C. andthe stable H. insolens enzyme showed no hydrolysis above 63° C. Theactivity of HJPlus in long-time cellulose hydrolysis assays exceededthat of all the parents at their respective optimal temperatures.

The CBH II library has fewer potential disruptions for several reasons.In addition to the higher identity of the CBH II parent sequences, thebarrel topology of the CBH II fold limits the number of long-rangecontacts that can be broken by recombination. Between-block contacts(heavy atoms within 4.5 Å) comprise only 27% (503/1831) of the total ina contact map derived from H. insolens structure 1ocn. When onlycounting contacts for which novel residue pairs are possible inchimeras, the inter-block total is reduced to 23% (68/294). Furthermore,most of these interactions are between residues on the protein surface,and the possibility of solvent screening further decreases the chancesof dramatic disruptive residue-residue interactions (FIG. 14a ). Oneexception, a buried interaction between positions 176 and 256, isillustrated in FIG. 14b . At this site, chimeras with B6P2 and eitherB5P1 or B5P3 pair Met173:Trp253 (larger amino acid than parental pairsMet176:Phe256 or Leu173:Trp253). Nevertheless, upon inspection of theparental crystallographic models, a steric clash at this position wasdeemed unlikely due to movement in the portion of the protein backbonewhich positions Trp253 and the intrinsic flexibility of Met side chains.Notably, one characterized chimera fits this pattern (13333232) and ismore stable than the parents (67° C.), in accord with the regressionmodel fit (68° C.)

Another mechanism by which coupling could arise, block structuraldivergence, does not depend on the presence of novel residue pairs atblock interfaces. Instead, as parental sequences diverge, intrinsicblock structures may diverge, hindering modular block transplants. Inthe case of the CBH II library, the high parent pair sequence identityvalues (82%, 66%, and 64%) suggest that only minor structure deviationsare likely (<1 Å RMSD). This possibility can be evaluated by comparingcrystallographic structures for H. insolens and H. jecorina CBH II (C.thermophilum CBH II lacks a crystal structure but is 82% identical to H.insolens). Aligning blocks from structures for each parent (1ocn and1cb2), generates low alpha carbon RMSD values (0.5, 0.5, 0.6, 0.5, 0.3,0.7, 0.3, and 0.4 Å RMSD). H. jecorina blocks superimposed onto H.insolens are illustrated in Supplemental FIG. 5c . To check forcontext-dependent effects an in silico structural recombination wasperformed, splicing each aligned block onto the opposing host structure.It is possible to construct non-clashing structural models (alphacarbons>3 Å apart) for all single-block substitution chimeras (e.g.,11112111 or 22122222), with the exception of a minor clash (2.65 Å) whenusing B7P2 (11111121) due to the Asn insertion between blocks 6 and 7(FIG. 14D).

Further experiments were performed to determine the contributions ofvarious blocks/segments to the chimera's stability and improvedthermostability and/or pH stability. Parent and chimeric genes encodingCBH II enzymes were cloned into yeast expression vectorYEp352/PGK91-1-αss and expression in synthetic dextrose casamino acids(SDCAA) media. For Avicel activity assays, yeast peptone dextrose (YPD)culture supernatants were brought to 1 mM phenylmethylsulfonylfluorideand 0.02% NaN₃ and used without concentration. CBH II enzyme activity inconcentrated SDCAA yeast culture supernatants was measured by addingdilutions of concentrated culture supernatant to 37.5 μL PASC and 225 μL50 mM sodium acetate, pH 4.8 and incubating for 2 hr at 50° C. Reducingsugar equivalents formed were determined via Nelson-Somogyi assay.

CBH II enzyme T₅₀ values were measured by adding concentrated CBH IISDCAA expression culture supernatant to 50 mM sodium acetate, pH 4.8 ata concentration giving A₅₂₀ of 0.5 as measured in the Nelson-Somogyireducing sugar assay after incubation with endoglucanase-treated PASC.200 μL CBH II enzyme/buffer mixtures were incubated in a water bath atthe temperature of interest for 10 minutes. After incubation, 37.5 μLendoglucanase-treated PASC and 62.5 μL of 50 mM sodium acetate wereadded, and hydrolysis was carried out for 2 hr at 50° C. The incubationtemperature at which the enzyme lost one-half of its activity wasdetermined by linear interpolation of the Nelson-Somogyi assay A₅₂₀values plotted versus temperature.

For long-time Avicel PH101 (Fluka) hydrolysis measurements, 0.3 μg ofpurified CBH II was incubated with 3 mg of Avicel in 270 μL of 50 mMsodium acetate, pH 4.8, in PCR tubes placed in a water bath for 16hours. Tubes were cooled in a room temperature water bath for 10minutes, centrifuged at 1000 g for 10 minutes and supernatants withdrawnfor reducing sugar analysis.

For estimation of CBH II activity in YPD expression culturesupernatants, supernatant volumes ranging from 2 mL to 40 mL were addedto 800 μL of 33 mg/mL Avicel suspended in 50 mM sodium acetate, pH 4.8in conical tubes. CBH IIs were allowed to bind Avicel at 4° C. for onehour, centrifuged at 2000 g for 2 minutes and washed twice with 50 mMsodium acetate, pH 4.8. After the second wash, CBH II-bound Avicel wasresuspended in 2.75 mL of sodium acetate buffer, split into 270 μLaliquots and incubated at 50° C. for 2.5 hours. Centrifugation andsupernatant reducing sugar analysis were carried out as above.

The Linear Regression package in Mathematica was used to fit CBH IIchimera T₅₀ data to a 17-parameter, block additive model and was alsoused for cross validation analysis. Block effects are reported relativeto a parent 1 (H. insolens CBH II) reference state with 16 parametersrepresenting substitution of each of the 8 blocks from parents 2 and 3.

Values of T₅₀, defined here as the temperature at which an enzyme loses50% of its activity during a ten-minute incubation, were determined forthe three parent cellobiohydrolases, 33 active CBH II chimeras fromprior experiments and 18 additional chimeras that qualitative stabilitymodeling predicted to be among the most thermostable, i.e. containingnone of the 7 predicted destabilizing blocks and either 3 or 4 of the 4predicted stabilizing blocks. All 51 chimera sequences are listed inTable 8. Re-culturing and re-concentrating all of the predictedthermostable chimeras previously classified as not secreted allowed forthe obtaining of sufficient amounts of 12112132, 13111132 and 13322332CBH IIs for T₅₀ determination. The complete set of T₅₀ values for thechimeras and parent CBH IIs is provided in Table 8. The amino acidsequences for all these CBH IIs appear in Table 7. All 31 predictedthermostable chimeras tested have T₅₀ values more than two degreeshigher than that of the most thermostable parent enzyme (64.8° C.). Thetable also identifies the Cys residue in block/domain 7 that can bemutated to a Ser to provide increased thermostability. Accordingly, thedisclosure provides polypeptide of any of the following sequenceswherein the underlined/italicized/bold Cys is substituted with a Serresidue and wherein the resulting polypeptide has improvedthermostability compared to a wild-type enzyme.

TABLE 7 Amino acid sequences for CBH II parent and chimeracatalytic domains shown in Table 8. Table also includes catalyticdomain for P. chrysosporium CBH II. All recombinant CBH IIs sharethe N-terminal CBM and linker from the native H. jecorina CBH II,CSSVWGQCGGQNWSGPTCCASGSTCVYSNDYYSQCLPGAASSSSSTRAASTTSRVSPTTSRSSSATPPPGSTTTRVPPVGSGTATYS (SEQ ID NO: 8).Parent 1 (H. insolens) (SEQ ID NO: 2)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAQFIVDQGRSGKQPTGQKEWGHWCNAIGTGFGMRPTANTGHQYVDAFVWVKPGGE

DGTSDTTAARYDYHCGLEDALKPAPE AGQWFNEYFIQLLRNANPPFParent 2 (H. jecorina) (SEQ ID NO: 4)GNPFVGVTPWANAYYASEVSSLAIPSLTGAMATAAAAVAKVPSFMWLDTLDKTPLMEQTLADIRTANKNGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDTIRQIVVEYSDIRTLLVIEPDSLANLVTNLGTPKCANAQSAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNGWNITSPPSYTQGNAVYNEKLYIHAIGPLLANHGWSNAFFITDQGRSGKQPTGQQQWGDWCNVIGTGFGIRPSANTGDSLLDSFVWVKPGGE

DGTSDSSAPRFDSHCALPDALQPAPQAGA WFQAYFVQLLTNANPSFLParent 3 (C. thermophilum) (SEQ ID NO: 6)GNPFSGVQLWANTYYSSEVHTLAIPSLSPELAAKAAKVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTSAARYDYHCGLSDALTPAPEAGQWFQAYFEQLLINANPPF P. chrysosporium CBH II (SEQ ID NO: 12)NNPWTGFQIFLSPYYANEVAAAAKQITDPTLSSKAASVANIPTFTWLDSVAKIPDLGTYLASASALGKSTGTKQLVQIVIYDLPDRDCAAKASNGEFSIANNGQANYENYIDQIVAQIQQFPDVRVVAVIEPDSLANLVTNLNVQKCANAKTTYLACVNYALTNLAKVGVYMYMDAGHAGWLGWPANLSPAAQLFTQVWQNAGKSPFIKGLATNVANYNALQAASPDPITQGNPNYDEIHYINALAPLLQQAGWDATFIVDQGRSGVQNIRQQWGDWCNIKGAGFGTRPTTNTGSQFIDSIVWVKPGGE

DGTSNSSSPRYDSTCSLPDAAQPAPEAGTW FQAYFQTLVSAANPPL 32333113 (SEQ ID NO: 13)GNPFSGVQLWANTYYSSEVHTLAIPSLSPELAAKAAKVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAQFIVDQGRSGKQPTGQKEWGHWCNAIGTGFGMRPTANTGHQYVDAFVWVKPGGE

DGTSDTSAARYDYHCGLSDALTPAPEAG QWFQAYFEQLLINANPPF 13111313 (SEQ ID NO: 14)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAQFIVDQGRSGKQPTGQKEWGHWCNAIGTGFGMRPTANTGHQYVDAFVWVKPGGE

DGTSDTSAARYDYHCGLSDALTPAPE AGQWFQAYFEQLLINANPPF 11313121 (SEQ ID NO: 15)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPNAFFITDQGRSGKQPTGQQQWGDWCNVIGTGFGIRPSANTGDSLLDSFVWVKPGGE

DGTSDTTAARYDYHCGLEDALKPAP EAGQWFNEYFIQLLRNANPPF 21131311 (SEQ ID NO: 16)GNPFVGVTPWANAYYASEVSSLAIPSLTGAMATAAAAVAKVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAQFIVDQGRSGKQPTGQKEWGHWCNAIGTGFGMRPTANTGHQYVDAFVWVKPGGE

DGTSDTTAARYDYHCGLEDALKPAPEA GQWFNEYFIQLLRNANPPF 31212111 (SEQ ID NO: 17)GNPFSGVQLWANTYYSSEVHTLAIPSLSPELAAKAAKVAEVPSFQWLDRNVTVDTLLVQTLSEIREANQAGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAQFIVDQGRSGKQPTGQKEWGHWCNAIGTGFGMRPTANTGHQYVDAFVWVKPGGE

DGTSDTTAARYDYHCGLEDALKPAPEAGQ WFNEYFIQLLRNANPPF 23233133 (SEQ ID NO: 18)GNPFVGVTPWANAYYASEVSSLAIPSLTGAMATAAAAVAKVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTSAARYDYHCGLSDALTPAPEAGQWFQAYFEQLLINANPPF 31311112 (SEQ ID NO: 19)GNPFSGVQLWANTYYSSEVHTLAIPSLSPELAAKAAKVAEVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAQFIVDQGRSGKQPTGQKEWGHWCNAIGTGFGMRPTANTGHQYVDAFVWVKPGGE

DGTSDSSAPRFDSHCALPDALQPAP QAGAWFQAYFVQLLTNANPSFL22212231 (SEQ ID NO: 20)GNPFVGVTPWANAYYASEVSSLAIPSLTGAMATAAAAVAKVPSFMWLDTLDKTPLMEQTLADIRTANKNGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNGWNITSPPSYTQGNAVYNEKLYIHAIGPLLANHGWSAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF 13231111 (SEQ ID NO: 21)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAQFIVDQGRSGKQPTGQKEWGHWCNAIGTGFGMRPTANTGHQYVDAFVWVKPGGE

DGTSDTTAARYDYHCGLEDALKPAPEAG QWFNEYFIQLLRNANPPF 12213111 (SEQ ID NO: 22)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAQFIVDQGRSGKQPTGQKEWGHWCNAIGTGFGMRPTANTGHQYVDAFVWVKPGGE

DGTSDTTAARYDYHCGLEDALKPAPEAGQ WFNEYFIQLLRNANPPF 12133333 (SEQ ID NO: 23)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTSAARYDYHCGLSDALTPAPEAGQWFQAYFEQLLINANPPF 33133132 (SEQ ID NO: 24)GNPFSGVQLWANTYYSSEVHTLAIPSLSPELAAKAAKVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 11332333 (SEQ ID NO: 25)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTSAARYDYHCGLSDALTPAPEAGQWFQAYFEQLLINANPPF 23311333 (SEQ ID NO: 26)GNPFVGVTPWANAYYASEVSSLAIPSLTGAMATAAAAVAKVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTSAARYDYHCGLSDALTPAPEAGQWFQAYFEQLLINANPPF 33213332 (SEQ ID NO: 27)GNPFSGVQLWANTYYSSEVHTLAIPSLSPELAAKAAKVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13333232 (SEQ ID NO: 28)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNGWNITSPPSYTQGNAVYNEKLYIHAIGPLLANHGWS_AKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 22232132 (SEQ ID NO: 29)GNPFVGVTPWANAYYASEVSSLAIPSLTGAMATAAAAVAKVPSFMWLDTLDKTPLMEQTLADIRTANKNGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 11113132 (SEQ ID NO: 30)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 21333331 (SEQ ID NO: 31)GNPFVGVTPWANAYYASEVSSLAIPSLTGAMATAAAAVAKVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF 21311131 (SEQ ID NO: 32)GNPFVGVTPWANAYYASEVSSLAIPSLTGAMATAAAAVAKVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF 12332331 (SEQ ID NO: 33)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF 13112332 (SEQ ID NO: 34)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 22311331 (SEQ ID NO: 35)GNPFVGVTPWANAYYASEVSSLAIPSLTGAMATAAAAVAKVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF 12111332 (SEQ ID NO: 36)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDT_LDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFD_AKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 12112332 (SEQ ID NO: 37)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDT_LDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDA_KFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 12131331 (SEQ ID NO: 38)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF 12131332 (SEQ ID NO: 39)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 12332332 (SEQ ID NO: 40)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 12111131 (SEQ ID NO: 41)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF 12311332 (SEQ ID NO: 42)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13332331 (SEQ ID NO: 43)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF 12132331 (SEQ ID NO: 44)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF 12132332 (SEQ ID NO: 45)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13332332 (SEQ ID NO: 46)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 12112132 (SEQ ID NO: 47)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13322332 (SEQ ID NO:48)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDTIRQIVVEYSDIRTLLVIEPDSLANLVTNLGTPKCANAQSAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13131332 (SEQ ID NO: 49)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 12331332 (SEQ ID NO: 50)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13312332 (SEQ ID NO: 51)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 11113332 (SEQ ID NO: 52)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13113132 (SEQ ID NO: 53)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 11112132 (SEQ ID NO: 54)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 12113132 (SEQ ID NO: 55)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYKELTVYALKQLNLPHVAMYMDAGHAGWLGWPANIQPAAELFAQIYRDAGRPAAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13132332 (SEQ ID NO: 56)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 11111132 (SEQ ID NO: 57)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLLVQTLSEIREANQAGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13331332 (SEQ ID NO: 58)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIRELLIQYSDIRTILVIEPDSLANMVTNMNVQKCSNAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13111132 (SEQ ID NO: 59)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPQYAAQIVVYDLPDRDCAAAASNGEWAIANNGVNNYKAYINRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 12222132 (SEQ ID NO: 60)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDTIRQIVVEYSDIRTLLVIEPDSLANLVTNLGTPKCANAQSAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSVSSPPPYTSPNPNYDEKHYIEAFRPLLEARGFPAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 12222332 (SEQ ID NO: 61)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFMWLDTLDKTPLMEQTLADIRTANKNGGNYAGQFVVYDLPDRDCAALASNGEYSIADGGVAKYKNYIDTIRQIVVEYSDIRTLLVIEPDSLANLVTNLGTPKCANAQSAYLECINYAVTQLNLPNVAMYLDAGHAGWLGWPANQDPAAQLFANVYKNASSPRALRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13311332 (SEQ ID NO: 62)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDAKFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDSSAPRFDSHCALPDALQPAPQAGAWFQAYFVQLLTNANPSFL 13311331 (SEQ ID NO: 63)GNPFEGVQLWANNYYRSEVHTLAIPQITDPALRAAASAVAEVPSFQWLDRNVTVDTLFSGTLAEIRAANQRGANPPYAGIFVVYDLPDRDCAAAASNGEWSIANNGANNYKRYIDRIREILISFSDVRTILVIEPDSLANMVTNMNVPKCSGAASTYRELTIYALKQLDLPHVAMYMDAGHAGWLGWPANIQPAAELFAKIYEDAGKPRAVRGLATNVANYNAWSIASPPSYTSPNPNYDEKHYIEAFAPLLRNQGFDA_KFIVDTGRNGKQPTGQLEWGHWCNVKGTGFGVRPTANTGHELVDAFVWVKPGGESDGTSDTTAARYDYHCGLEDALKPAPEAGQWFNEYFIQLLRNANPPF

TABLE 8 Two independent duplicate T₅₀ values (° C.) for parent CBH IIs,23 original sample set CBH II chimeras and predicted thermostable CBH IIchimeras. The 18 chimeras synthesized for this work are preceded by anasterisk. Sample Set Chimeras & Parents Predicted Thermostable ChimerasSequence T₅₀ (1) T₅₀ (2) MeanT₅₀ Sequence T₅₀ (1) T₅₀ (2) MeanT₅₀32333113 52 51 51.5 12332331 66.5 67 66.8 13111313 56 53.5 54.8*13112332 67 67 67 11313121 55 55.5 55.3 22311331 68 68 68 21131311 57.557 57.3 *12111332 68 68 68 31212111 59 58 58.5 *12112332 68.5 67.5 68Parent 2 60 58 59 12131331 68.5 69 68.8 23233133 61 61 61 *12131332 7067.5 68.8 31311112 60 62 61 *12332332 69 69 69 22212231 63 61 6212111131 70 68.5 69.3 13231111 63 6.5 63.3 12311332 70 69 69.5 1221311163 63.5 63.3 13332331 70 69 69.5 Parent 3 63.5 64.5 64 12132331 70.5 6969.8 12133333 64 64 64 *12132332 70.5 69 69.8 Parent 1 64 65.5 64.8*13332332 69.5 70 69.8 33133132 65 66 65 12112132 71 68.5 69.8 1133233364.5 66 65.3 13322332 71 68.5 69.8 23311333 65 66 65.5 *13131332 70 7070 33213332 66 66 66 *12331332 71 69 70 13333232 67.5 67 67.3 *1331233270 70 70 22232132 68 68 68 *11113332 69.5 70.5 70 11113132 71.5 71 71.3*13113132 70.5 69.5 70 21333331 73.5 75.5 74.5 *11112132 70.5 70 70.321311131 75.5 75.5 75 *12113132 70.5 70.5 70.5 *13132332 69.5 71.5 70.5*11111132 71 70.5 70.8 13331332 72 70 71 *13111132 72 69.5 71.3*12222132 72.5 70 71.3 12222332 72 69.5 71.3 13311332 71 71.5 71.713311331 73.5 72.5 73

Applying linear regression to the sequence-stability data resulted in aten-parameter model that fit the observed T₅₀ values with R²=0.88 (FIG.8). To better estimate the predictive capacity of the regression modeloutside the training set, an eleven-fold cross-validation was performedresulting in a R² of 0.57, where removal of two outliers, (11313121 and22222222) increases the cross validation R² to 0.76. The regressionmodel model uses the most stable parent 1 (H. insolens) as the referencestate T₅₀ and includes nine additional terms having p values 0.1. Themodel parameters (Table 9) show that a single block, block 7 from parent3 (B7P3), is by far the strongest contributor to chimera thermostabilityrelative to H. insolens CBH II. This block from C. thermophilum CBH IIcontributes approximately 8.5° C. to the stability of chimeras thatcontain it. Two of the 8 remaining blocks with p values 0.1 were foundto make smaller stability contributions, of 1.2° C. and 2.7° C., whereasthe other six decrease stability.

TABLE 9 T₅₀ linear regression model parameters and p-values. Parametervalues with p ≦ 0.1, used to calculate the regression fit line of FIG.1, appear in bold. Block effects are reported relative to a parent 1 (H.insolens CBH II) reference state with 16 parameters representingsubstitution of each of the 8 blocks from parents 2 and 3. ParameterBlock Value p-value Parent1 62.8 0.00 B12 −0.9 0.35 B13 −3.5 0.00 B22−1.7 0.06 B23 −1.1 0.25 B32 0.5 0.68 B33 1.2 0.10 B42 2.7 0.05 B43 0.00.99 B52 −1.3 0.10 B53 −0.6 0.50 B62 −3.5 0.02 B63 −0.7 0.37 B72 −3.80.05 B73 8.5 0.00 B82 0.0 1.00 B83 −5.6 0.00

Alignment of the B7P1 and B7P3 sequences (FIG. 10) shows that block 7differs at 10 out of 56 amino acid positions in the H. insolens and C.thermophilum enzymes. In the background of the chimera with the highestT₅₀ value, 21311131, each residue in B7P3 (segment 7 of parent 3 (SEQ IDNO:6)) was individually mutated to the corresponding residue in B7P1(segment 7 of parent 1 (SEQ ID NO:2)) and determined T₅₀ values for eachof the point mutants was obtained. A mutation, S313C, markedly alteredthe chimera's thermostability: this single mutation reduced the T₅₀ of21311131 by approximately 10° C. (FIG. 11).

To study the effect of the reverse mutation in different backgrounds,genes for the H. insolens and H. jecorina parent CBH IIs encoding theC313S substitution (C314S in H. insolens and C311S in H. jecorina) wereconstructed, expressed, and the enzymes' T₅₀ values were determined. Thestabilities of chimeras 11111131 and 22222232, in which the stabilizingB7P3 is substituted into the wildtype H. insolens and H. jecorinaenzymes were also quantified. Both the B7P3 block substitution and theCys-Ser point mutation markedly stabilized the parent CBH IIs; thelargest effect was a ˜8° C. increase in T₅₀ for H. jecorina CBH IIcontaining the C311S substitution (FIG. 12). The Cys-Ser mutation wasalso tested in two chimeras, 31311112 and 13231111, that did not containB7P3 as well as in a homologous CBH II (from Phanerochaetechrysosporium) which was not in the recombination parent set. The P.chrysosporium CBH II catalytic domain is only 55-56% identical to theparent CBH II catalytic domains. All of these enzymes were stabilized bythe Cys-Ser substitution; the P. chrysosporium CBH II was stabilized bya remarkable 10° C. (FIG. 13).

Eight of the thermostable CBH II chimeras and the parent enzymescontaining the equivalent C313S mutation were His6-tagged and purifiedso that their specific activities could be determined. As shown in Table10A, the specific activities, as measured on amorphous cellulose (PASC)at 50° C., for these chimeras and native enzymes containing the Cys-Sermutation are similar to those of the wildtype parents. Thus theincreased thermostability does not come at the expense of specificactivity.

TABLE 10A Specific activity values (μg glucose reducing sugarequivalent/(μg CBH II enzyme × min × 10²)) for native, point mutant andselected thermostable chimeric CBH IIs. Error bars show standard errors,where standard error is defined as standard dev/sqrt (n), for threereplicates. 2-hr reaction, 3 mg enzyme/g PASC, 50° C., 25 mM sodiumacetate, pH 4.8. Specific Activity μg Reducing Sugar/(μg CBH II EnzymeEnzyme × min) × 10² Humicola insolens (Parent 1) 5.3 +/− 0.5 Hypocreajecorina (Parent 2) 8.4 +/− 0.4 Chaetomium thermophilum (Parent 3) 4.8+/− 0.3 Phanerochaete chyrsosporium 7.7 +/− 0.3 Humicola insolens C314S5.3 +/− 0.9 Hypocrea jecorina C311S 7.8 +/− 0.5 Phanerochaetechyrsosporium C311S 8.5 +/− 0.1 HJPlus (Chimera 12222332) 9.6 +/− 0.8Chimera 13111132 8.5 +/− 0.3 Chimera 22222232 7.7 +/− 0.3 Chimera13311332 6.8 +/− 0.6 Chimera 13311331 6.2 +/− 0.3 Chimera 11111131 6.1+/− 0.9 Chimera 13112332 5.6 +/− 0.4 Chimera 21311131 5.5 +/− 0.3Chimera 11113132 5.3 +/− 0.5 Chimera 21333331 3.8 +/− 0.4

TABLE 10B total activity in both synthetic (SDCAA) and rich (YPD)expression culture media supernatants for H. jecorina and H. insolenswild type, C313S point mutant and B7P3 block susbstitution CBH IIs.Values presented are μg glucose/mL cellulase activity assay per mL ofexpression culture supernatant CBH II equivalent added to cellulaseactivity assay. For SDCAA cultures, concentrated SDCAA culturesupernatants were used and activity toward phosphoric acid swollencellulose (1 mg/mL) at 50° C. for 100 minutes in 50 mM sodium acetate,pH 4.8, was measured. YPD supernatant CBH II was concentrated by bindingto avicel and activity toward avicel (15 mg/mL) at 55° C. for 150minutes in 50 mM sodium acetate, pH 4.8, was measured. SDCAA SDCAA SDCAAYPD YPD CBH II (1) (2) Mean YPD (1) (2) Mean H. jecorina 19 17 18 0.40.4 0.4 H. jeco C311S 50 43 47 6.1 5.6 5.9 H. jeco B7P3 35 33 34 3.9 3.63.8 H. insolens 73 83 78 6.2 6.0 6.1 H. inso C314S 100 97 98 8.8 8.0 8.4H. inso B7P3 39 42 40 4.4 4.1 4.2

These same eight thermostable chimeras (T₅₀ 2-10° C. higher than themost stable parent) were then tested for activity on crystallinecellulose during a 16-hour incubation over a range of temperatures,including temperatures where the parent enzymes exhibit little or noactivity. FIG. 9a shows that 7 of 8 tested thermostable chimeras weremaximally active toward Avicel at 60-65° C., with all 8 chimerasretaining activity at 70° C., the highest temperature tested. Incontrast, the three parent CBH IIs show maximum activity at 50° C. andare either completely or almost completely inactive at 70° C.Additionally, the seven chimeras with increased optimum activitytemperatures hydrolyze significantly more Avicel than any of the parentCBH II enzymes. As shown in FIG. 9b , similar behaviors are observed forthe H. insolens and H. jecorina parents containing the Cys-Ser pointmutation. The Cys-Ser point mutation also increased the Avicelhydrolysis and maximum operating temperature for the P. chrysosporiumCBH II. The P3B7 block substitution, which was made in the H. insolensand H. jecorina parents, increased both the operating temperature andhydrolysis of the H. insolens CBH II but, despite increasing maximumoperating temperature, did not improve overall cellulose hydrolysis bythe H. jecorina enzyme.

Low (<1 mg/L) secretion of wildtype H. jecorina CBH II was observed fromthe heterologous S. cerevisiae expression host. The C311S mutation inthe wildtype H. jecorina CBH II enzyme markedly increases total secretedCBH II activity (Table 11). In synthetic (SDCAA) medium, the C311S andB7P3 substitutions increase H. jecorina CBH II total secreted activityby a factor of two, while in rich (YPD) medium the activity increase istenfold. For the H. insolens CBH II parent, which is expressed at muchhigher levels than the other two parent CBH IIs, the C314S mutationincreased secreted activity by a factor of ˜1.5 whereas the B7P3 blocksubstitution decreased it. Because the H. insolens and H. jecorinawildtype and Cys-Ser mutants all have similar specific activities (Table10), the increase in total secreted cellulase activity is the result ofimproved secretion of the functional enzyme. A correlation between S.cerevisiae heterologous protein secretion and protein stability has beenobserved, suggesting that the increased secretion of the Cys-Ser mutantCBH IIs might reflect their higher stabilities.

TABLE 11 Specific activity values (μg glucose reducing sugarequivalent/(μg CBH II enzyme × min × 10²)) for native, point mutant andselected thermostable chimeric CBH IIs. Error bars show standard errors,where standard error is defined as standard dev/sqrt (n), for threereplicates. 2-hr reaction, 3 mg enzyme/g PASC, 50° C., 25 mM sodiumacetate, pH 4.8. Specific Activity μg Reducing Sugar/(μg CBH II EnzymeEnzyme × min) × 10² Humicola insolens (Parent 1) 5.3 +/− 0.5 Hypocreajecorina (Parent 2) 8.4 +/− 0.4 Chaetomium thermophilum (Parent 3) 4.8+/− 0.3 Phanerochaete chyrsosporium 7.7 +/− 0.3 Humicola insolens C314S5.3 +/− 0.9 Hypocrea jecorina C311S 7.8 +/− 0.5 Phanerochaetechyrsosporium C311S 8.5 +/− 0.1 HJPlus (Chimera 12222332) 9.6 +/− 0.8Chimera 13111132 8.5 +/− 0.3 Chimera 22222232 7.7 +/− 0.3 Chimera13311332 6.8 +/− 0.6 Chimera 13311331 6.2 +/− 0.3 Chimera 11111131 6.1+/− 0.9 Chimera 13112332 5.6 +/− 0.4 Chimera 21311131 5.5 +/− 0.3Chimera 11113132 5.3 +/− 0.5 Chimera 21333331 3.8 +/− 0.4

To model the Cys-Ser mutation, the high-resolution H. insolens CBH IIloon crystal structure was used. First, the hydrogen bond network wasoptimized with REDUCE. Cys314 was predicted to form a hydrogen bond tothe carbonyl of Pro 339. To confirm this prediction, sidechain packingwas optimized using the modeling platform SHARPEN. Ser314 is predictedto make the similar interactions to Cys314, resulting in strongerhydrogen bonding and a more favorable geometry (FIG. 14).

A number of effects might explain why the Cys-Ser mutation stabilizes abroad range of CBH IIs, including native CBH IIs and chimeras. Cys andSer are similar (though not isosteric), and these two amino acidsdominate sequence alignments at this position compared to otheralternatives. The hydrogen bonding partners for this residue arebackbone elements (the amide of Gly316 and the carbonyl of Pro339 andare therefore less likely to be dependent on third-party amino acidvariations. Furthermore, the immediate neighboring side chains for thispocket (Asn283, Pro339, Phe345) are conserved among all four native CBHII cellulases studied.

The high-resolution (1.3 Å) H. insolens crystal structure (pdb entry1ocn6) shows that Cys314 is part of a hydrogen bonding network (FIG.15). The increased hydrogen bonding capacity of Ser relative to Cys maysuggest a role for stronger hydrogen bonding interactions in thestabilization. The crystal structure also suggests that Ser may bepreferred for steric reasons. Specifically, when the Cys side chain isrebuilt with canonical bond angles, a 6° bend is removed and Cys ispushed closer to the carbonyl of Pro339, creating an unfavorable stericinteraction.

An alignment of the 196 protein sequences sharing the greatest identityto the H. jecorina CBH II. Fifty-four of the 250 most identicalsequences were excluded from the alignment due to redundancy (i.e. pointmutants for structural studies or >95% identical isoforms). There is abias in favor of Ser311: 158 sequences have Ser, 20 have Ala, 10 haveCys, 5 have a deletion, and 3 have Gly. However, there are 42 otherpositions where the most frequent choice occurs with greater than twicethe frequency of the H. jecorina amino acid.

The large stabilizing effect of the Cys-Ser mutation raises thepossibility that Ser at this position is a global indicator of nativecellulase thermostability. However, the T₅₀ of 64.8° C. for H. insolensCBH II, which features Cys at this position, is greater than that of theC. thermophilum CBH II (64.0° C.), indicating that Ser is not the onlystability determinant.

Thermostability is not the only property of interest for industrialcellulases. Specific activity, changes to cellulose binding, and effectson expression and product inhibition are all important as well. Thechimeras and data herein demonstrate that recombination yields CBH IIchimeras whose improved thermostability comes without cost to specificactivity measured in short-time (e.g., 2-hour) cellulose hydrolysisassays. Similar observations were made for CBH IIs containing thethermostabilizing Cys-Ser mutation. In long-time hydrolysis assays,several of the CBH II chimeras and all three tested Cys-Ser mutant CBHIIs hydrolyzed more cellulose than the native CBH IIs. This superiorperformance is likely the result of having specific activity comparableto that of the parent CBH IIs along with greater thermostability thatallows the enzyme to continue to function for longer time at theelevated temperatures. Because these assays were carried out with equalamounts of purified parent, chimera and Cys-Ser mutant enzymes, theobserved high temperature hydrolysis improvements are not the result ofincreased secretion from the S. cerevisiae expression host. Thethermostable chimeras and the Cys-Ser mutants may therefore prove to beuseful components of enzyme formulations for cellulose degradation.

While various specific embodiments have been illustrated and described,it will be appreciated that various changes can be made withoutdeparting from the spirit and scope of the invention(s).

1. (canceled)
 2. A recombinant polypeptide selected from the groupconsisting of a, polypeptide comprising a sequence that is (a) identicalto SEQ ID NO:67 and having a C400S mutation; (b) is at least 85%identical to SEQ ID NO:68 and having a C400S mutation; (c) is at least85% identical to SEQ ID NO:69 and having a C400S mutation; (d) is atleast 85% identical to SEQ ID NO:70 and having a C400S mutation; (e) isat least 85% identical to SEQ ID NO:71 and having a C400S mutation; (f)is at least 85% identical to SEQ ID NO:72 and having a C400S mutation;(d) is at least 85% identical to SEQ ID NO:73 and having a C400Smutation; (h) is at least 85% identical to SEQ ID NO:74 and having aC400S mutation; (i) is at least 85% identical to SEQ ID NO:75 and havinga C400S mutation; (j) is at least 85% identical to SEQ ID NO:76 andhaving a C407S mutation; (k) is at least 85% identical to SEQ ID NO:77and having a C394S mutation; and (l) is at least 85% identical to SEQ IDNO:78 and having a C412S, wherein the foregoing polypeptides havecellulase activity and improved thermostability compared to theircorresponding parental (wild-type) protein lacking a Cys→Ser mutation.3. The recombinant polypeptide of claim 2, wherein the polypeptide hasfrom 1-30 conservative amino acid substitutions except at the positionidentified below wherein a C→S substitution is present: SEQ ID NO:67comprising a C400S; SEQ ID NO:68 comprising a C400S; SEQ ID NO:69comprising a C400S; SEQ ID NO:70 comprising a C400S; SEQ ID NO:71comprising a C400S; SEQ ID NO:72 comprising a C400S; SEQ ID NO:73comprising a C400S; SEQ ID NO:74 comprising a C400S; SEQ ID NO:75comprising a C400S; SEQ ID NO:76 comprising a C407S; SEQ ID NO:77comprising a C394S, or SEQ ID NO:78 comprising a C412S. 4-7. (canceled)8. A polynucleotide encoding a polypeptide of claim
 2. 9. A vectorcomprising a polynucleotide of claim
 8. 10. A host cell comprising thepolynucleotide of claim
 8. 11. A host cell comprising the vector ofclaim
 9. 12. An enzymatic preparation comprising a polypeptide of claim2.
 13. An enzymatic preparation comprising a polypeptide produced by ahost cell of claim
 10. 14. A method of treating a biomass comprisingcellulose, the method comprising contacting the biomass with apolypeptide of claim
 2. 15. A method of treating a biomass comprisingcellulose, the method comprising contacting the biomass with anenzymatic preparation of claim 12.